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73072 results found
| D31.60 | Benign neoplasm of unspecified site of unspecified orbit |
| D31.61 | Benign neoplasm of unspecified site of right orbit |
| D31.62 | Benign neoplasm of unspecified site of left orbit |
| D31.90 | Benign neoplasm of unspecified part of unspecified eye |
| D31.91 | Benign neoplasm of unspecified part of right eye |
| D31.92 | Benign neoplasm of unspecified part of left eye |
| D32.0 | Benign neoplasm of cerebral meninges |
| D32.1 | Benign neoplasm of spinal meninges |
| D32.9 |
Benign neoplasm of meninges, unspecified
Includes: Meningioma NOS |
| D33.0 |
Benign neoplasm of brain, supratentorial
Includes: Benign neoplasm of cerebral ventricle Benign neoplasm of cerebrum Benign neoplasm of frontal lobe Benign neoplasm of occipital lobe Benign neoplasm of parietal lobe Benign neoplasm of temporal lobe Excludes 1: benign neoplasm of fourth ventricle (D33.1) |
| D33.1 |
Benign neoplasm of brain, infratentorial
Includes: Benign neoplasm of brain stem Benign neoplasm of cerebellum Benign neoplasm of fourth ventricle |
| D33.2 | Benign neoplasm of brain, unspecified |
| D33.3 |
Benign neoplasm of cranial nerves
Includes: Benign neoplasm of olfactory bulb |
| D33.4 | Benign neoplasm of spinal cord |
| D33.7 | Benign neoplasm of other specifiedparts of central nervous system |
| D33.9 |
Benign neoplasm of central nervoussystem, unspecified
Includes: Benign neoplasm of nervous system (central) NOS |
| D34 | Benign neoplasm of thyroid gland |
| D35.00 | Benign neoplasm of unspecified adrenal gland |
| D35.01 | Benign neoplasm of right adrenal gland |
| D35.02 | Benign neoplasm of left adrenal gland |
| D35.1 | Benign neoplasm of parathyroid gland |
| D35.2 | Benign neoplasm of pituitary gland |
| D35.3 | Benign neoplasm of craniopharyngeal duct |
| D35.4 | Benign neoplasm of pineal gland |
| D35.5 | Benign neoplasm of carotid body |
| D35.6 |
Benign neoplasm of aortic body andother paraganglia
Includes: Benign tumor of glomus jugulare |
| D35.7 | Benign neoplasm of other specifiedendocrine glands |
| D35.9 |
Benign neoplasm of endocrine gland, unspecified
Includes: Benign neoplasm of unspecified endocrine gland |
| D36.0 |
Benign neoplasm of lymph nodes
Excludes 1: lymphangioma (D18.1) |
| D36.10 | Benign neoplasm of peripheral nerves and autonomic nervous system, unspecified |
| D36.11 | Benign neoplasm of peripheral nerves and autonomic nervous system of face, head, and neck |
| D36.12 | Benign neoplasm of peripheral nerves and autonomic nervous system, upper limb, including shoulder |
| D36.13 | Benign neoplasm of peripheral nerves and autonomic nervous system of lower limb, including hip |
| D36.14 | Benign neoplasm of peripheral nerves and autonomic nervous system of thorax |
| D36.15 | Benign neoplasm of peripheral nerves and autonomic nervous system of abdomen |
| D36.16 | Benign neoplasm of peripheral nerves and autonomic nervous system of pelvis |
| D36.17 | Benign neoplasm of peripheral nerves and autonomic nervous system of trunk, unspecified |
| D36.7 |
Benign neoplasm of other specifiedsites
Includes: Benign neoplasm of back NOS Benign neoplasm of nose NOS |
| D36.9 | Benign neoplasm, unspecified site |
| D3A.00 |
Benign carcinoid tumor of unspecified site
Includes: Carcinoid tumor NOS |
| D3A.010 | Benign carcinoid tumor of the duodenum |
| D3A.011 | Benign carcinoid tumor of the jejunum |
| D3A.012 | Benign carcinoid tumor of the ileum |
| D3A.019 | Benign carcinoid tumor of the small intestine, unspecified portion |
| D3A.020 | Benign carcinoid tumor of the appendix |
| D3A.021 | Benign carcinoid tumor of the cecum |
| D3A.022 | Benign carcinoid tumor of the ascending colon |
| D3A.023 | Benign carcinoid tumor of the transverse colon |
| D3A.024 | Benign carcinoid tumor of the descending colon |
| D3A.025 | Benign carcinoid tumor of the sigmoid colon |
| D3A.026 | Benign carcinoid tumor of the rectum |
| D3A.029 |
Benign carcinoid tumor of the large intestine, unspecified portion
Includes: Benign carcinoid tumor of the colon NOS |
| D3A.090 | Benign carcinoid tumor of the bronchus and lung |
| D3A.091 | Benign carcinoid tumor of the thymus |
| D3A.092 | Benign carcinoid tumor of the stomach |
| D3A.093 | Benign carcinoid tumor of the kidney |
| D3A.094 | Benign carcinoid tumor of the foregut, unspecified |
| D3A.095 | Benign carcinoid tumor of the midgut, unspecified |
| D3A.096 | Benign carcinoid tumor of the hindgut, unspecified |
| D3A.098 | Benign carcinoid tumors of other sites |
| D3A.8 |
Other benign neuroendocrine tumors
Includes: Neuroendocrine tumor NOS |
| D37.01 |
Neoplasm of uncertain behavior oflip
Includes: Neoplasm of uncertain behavior of vermilion border of lip |
| D37.02 | Neoplasm of uncertain behavior oftongue |
| D37.030 | Neoplasm of uncertain behavior ofthe parotid salivary glands |
| D37.031 | Neoplasm of uncertain behavior ofthe sublingual salivary glands |
| D37.032 | Neoplasm of uncertain behavior ofthe submandibular salivary glands |
| D37.039 | Neoplasm of uncertain behavior ofthe major salivary glands, unspecified |
| D37.04 |
Neoplasm of uncertain behavior ofthe minor salivary glands
Includes: Neoplasm of uncertain behavior of submucosal salivary glands of lip Neoplasm of uncertain behavior of submucosal salivary glands of cheek Neoplasm of uncertain behavior of submucosal salivary glands of hard palate Neoplasm of uncertain behavior of submucosal salivary glands of soft palate |
| D37.05 |
Neoplasm of uncertain behavior ofpharynx
Includes: Neoplasm of uncertain behavior of aryepiglottic fold of pharynx NOS Neoplasm of uncertain behavior of hypopharyngeal aspect of aryepiglottic fold of pharynx Neoplasm of uncertain behavior of marginal zone of aryepiglottic fold of pharynx |
| D37.09 | Neoplasm of uncertain behavior ofother specified sites of the oral cavity |
| D37.1 | Neoplasm of uncertain behavior ofstomach |
| D37.2 | Neoplasm of uncertain behavior ofsmall intestine |
| D37.3 | Neoplasm of uncertain behavior ofappendix |
| D37.4 | Neoplasm of uncertain behavior ofcolon |
| D37.5 |
Neoplasm of uncertain behavior ofrectum
Includes: Neoplasm of uncertain behavior of rectosigmoid junction |
| D37.6 |
Neoplasm of uncertain behavior ofliver, gallbladder and bile ducts
Includes: Neoplasm of uncertain behavior of ampulla of Vater |
| D37.8 |
Neoplasm of uncertain behavior ofother specified digestive organs
Includes: Neoplasm of uncertain behavior of anal canal Neoplasm of uncertain behavior of anal sphincter Neoplasm of uncertain behavior of anus NOS Neoplasm of uncertain behavior of esophagus Neoplasm of uncertain behavior of intestine NOS Neoplasm of uncertain behavior of pancreas Excludes 1: neoplasm of uncertain behavior of anal margin (D48.5) neoplasm of uncertain behavior of anal skin (D48.5) neoplasm of uncertain behavior of perianal skin (D48.5) |
| D37.9 | Neoplasm of uncertain behavior ofdigestive organ, unspecified |
| D38.0 |
Neoplasm of uncertain behavior oflarynx
Includes: Neoplasm of uncertain behavior of aryepiglottic fold or interarytenoid fold, laryngeal aspect Neoplasm of uncertain behavior of epiglottis (suprahyoid portion) Excludes 1: neoplasm of uncertain behavior of aryepiglottic fold or interarytenoid fold NOS (D37.05) neoplasm of uncertain behavior of hypopharyngeal aspect of aryepiglottic fold (D37.05) neoplasm of uncertain behavior of marginal zone of aryepiglottic fold (D37.05) |
| D38.1 | Neoplasm of uncertain behavior oftrachea, bronchus and lung |
| D38.2 | Neoplasm of uncertain behavior ofpleura |
| D38.3 | Neoplasm of uncertain behavior ofmediastinum |
| D38.4 | Neoplasm of uncertain behavior ofthymus |
| D38.5 |
Neoplasm of uncertain behavior ofother respiratory organs
Includes: Neoplasm of uncertain behavior of accessory sinuses Neoplasm of uncertain behavior of cartilage of nose Neoplasm of uncertain behavior of middle ear Neoplasm of uncertain behavior of nasal cavities Excludes 1: neoplasm of uncertain behavior of ear (external) (skin) (D48.5) neoplasm of uncertain behavior of nose NOS (D48.7) neoplasm of uncertain behavior of skin of nose (D48.5) |
| D38.6 | Neoplasm of uncertain behavior ofrespiratory organ, unspecified |
| D39.0 | Neoplasm of uncertain behavior ofuterus |
| D39.10 | Neoplasm of uncertain behavior ofunspecified ovary |
| D39.11 | Neoplasm of uncertain behavior ofright ovary |
| D39.12 | Neoplasm of uncertain behavior ofleft ovary |
| D39.2 |
Neoplasm of uncertain behavior ofplacenta
Includes: Chorioadenoma destruens Invasive hydatidiform mole Malignant hydatidiform mole Excludes 1: hydatidiform mole NOS (O01.9) |
| D39.8 |
Neoplasm of uncertain behavior ofother specified female genital organs
Includes: Neoplasm of uncertain behavior of skin of female genital organs |
| D39.9 | Neoplasm of uncertain behavior offemale genital organ, unspecified |
| D40.0 | Neoplasm of uncertain behavior ofprostate |
| D40.10 | Neoplasm of uncertain behavior ofunspecified testis |
| D40.11 | Neoplasm of uncertain behavior ofright testis |
| D40.12 | Neoplasm of uncertain behavior ofleft testis |
| D40.8 |
Neoplasm of uncertain behavior ofother specified male genital organs
Includes: Neoplasm of uncertain behavior of skin of male genital organs |
| D40.9 | Neoplasm of uncertain behavior ofmale genital organ, unspecified |
| D41.00 | Neoplasm of uncertain behavior ofunspecified kidney |
| D41.01 | Neoplasm of uncertain behavior ofright kidney |
| D41.02 | Neoplasm of uncertain behavior ofleft kidney |
| D41.10 | Neoplasm of uncertain behavior ofunspecified renal pelvis |
| D41.11 | Neoplasm of uncertain behavior ofright renal pelvis |
| D41.12 | Neoplasm of uncertain behavior ofleft renal pelvis |
| D41.20 | Neoplasm of uncertain behavior ofunspecified ureter |
| D41.21 | Neoplasm of uncertain behavior ofright ureter |
| D41.22 | Neoplasm of uncertain behavior ofleft ureter |
| D41.3 | Neoplasm of uncertain behavior ofurethra |
| D41.4 | Neoplasm of uncertain behavior ofbladder |
| D41.8 | Neoplasm of uncertain behavior ofother specified urinary organs |
| D41.9 | Neoplasm of uncertain behavior ofunspecified urinary organ |
| D42.0 | Neoplasm of uncertain behavior ofcerebral meninges |
| D42.1 | Neoplasm of uncertain behavior ofspinal meninges |
| D42.9 | Neoplasm of uncertain behavior ofmeninges, unspecified |
| D43.0 |
Neoplasm of uncertain behavior ofbrain, supratentorial
Includes: Neoplasm of uncertain behavior of cerebral ventricle Neoplasm of uncertain behavior of cerebrum Neoplasm of uncertain behavior of frontal lobe Neoplasm of uncertain behavior of occipital lobe Neoplasm of uncertain behavior of parietal lobe Neoplasm of uncertain behavior of temporal lobe Excludes 1: neoplasm of uncertain behavior of fourth ventricle (D43.1) |
| D43.1 |
Neoplasm of uncertain behavior ofbrain, infratentorial
Includes: Neoplasm of uncertain behavior of brain stem Neoplasm of uncertain behavior of cerebellum Neoplasm of uncertain behavior of fourth ventricle |
| D43.2 | Neoplasm of uncertain behavior ofbrain, unspecified |
| D43.3 | Neoplasm of uncertain behavior ofcranial nerves |
| D43.4 | Neoplasm of uncertain behavior ofspinal cord |
| D43.8 | Neoplasm of uncertain behavior ofother specified parts of central nervous system |
| D43.9 |
Neoplasm of uncertain behavior ofcentral nervous system, unspecified
Includes: Neoplasm of uncertain behavior of nervous system (central) NOS |
| D44.0 | Neoplasm of uncertain behavior ofthyroid gland |
| D44.10 | Neoplasm of uncertain behavior ofunspecified adrenal gland |
| D44.11 | Neoplasm of uncertain behavior ofright adrenal gland |
| D44.12 | Neoplasm of uncertain behavior ofleft adrenal gland |
| D44.2 | Neoplasm of uncertain behavior ofparathyroid gland |
| D44.3 | Neoplasm of uncertain behavior ofpituitary gland |
| D44.4 | Neoplasm of uncertain behavior ofcraniopharyngeal duct |
| D44.5 | Neoplasm of uncertain behavior ofpineal gland |
| D44.6 | Neoplasm of uncertain behavior ofcarotid body |
| D44.7 | Neoplasm of uncertain behavior ofaortic body and other paraganglia |
| D44.9 | Neoplasm of uncertain behavior ofunspecified endocrine gland |
| D45 |
Polycythemia vera
Excludes 1: familial polycythemia (D75.0) secondary polycythemia (D75.1) |
| D46.0 |
Refractory anemia without ring sideroblasts, so stated
Includes: Refractory anemia without sideroblasts, without excess of blasts |
| D46.1 |
Refractory anemia with ring sideroblasts
Includes: RARS |
| D46.20 |
Refractory anemia with excess of blasts, unspecified
Includes: RAEB NOS |
| D46.21 |
Refractory anemia with excess of blasts 1
Includes: RAEB 1 |
| D46.22 |
Refractory anemia with excess of blasts 2
Includes: RAEB 2 |
| D46.A | Refractory cytopenia with multilineage dysplasia |
| D46.B |
Refractory cytopenia with multilineage dysplasia and ring sideroblasts
Includes: RCMD RS |
| D46.C |
Myelodysplastic syndrome with isolated del(5q) chromosomal abnormality
Includes: Myelodysplastic syndrome with 5q deletion 5q minus syndrome NOS |
| D46.4 | Refractory anemia, unspecified |
| D46.Z |
Other myelodysplastic syndromes
Excludes 1: chronic myelomonocytic leukemia (C93.1-) |
| D46.9 |
Myelodysplastic syndrome, unspecified
Includes: Myelodysplasia NOS |
| D47.01 |
Cutaneous mastocytosis
Includes: Diffuse cutaneous mastocytosis Maculopapular cutaneous mastocytosis Solitary mastocytoma Telangiectasia macularis eruptiva perstans Urticaria pigmentosa Excludes 1: congenital (diffuse) (maculopapular) cutaneous mastocytosis (Q82.2) congenital urticaria pigmentosa (Q82.2) extracutaneous mastocytoma (D47.09) |
| D47.02 |
Systemic mastocytosis
Includes: Indolent systemic mastocytosis Isolated bone marrow mastocytosis Smoldering systemic mastocytosis Systemic mastocytosis, with an associated hematological non-mast cell lineage disease (SM-AHNMD) Excludes 1: aggressive systemic mastocytosis (C96.21) mast cell leukemia (C94.3-) |
| D47.09 |
Other mast cell neoplasms of uncertain behavior
Includes: Extracutaneous mastocytoma Mast cell tumor NOS Mastocytoma NOS Mastocytosis NOS |
| D47.1 |
Chronic myeloproliferative disease
Includes: Chronic neutrophilic leukemia Myeloproliferative disease, unspecified Excludes 1: atypical chronic myeloid leukemia BCR/ABL-negative (C92.2-) chronic myeloid leukemia BCR/ABL-positive (C92.1-) myelofibrosis NOS (D75.81) myelophthisic anemia (D61.82) myelophthisis (D61.82) secondary myelofibrosis NOS (D75.81) |
| D47.2 |
Monoclonal gammopathy
Includes: Monoclonal gammopathy of undetermined significance [MGUS] |
| D47.3 |
Essential (hemorrhagic) thrombocythemia
Includes: Essential thrombocytosis Idiopathic hemorrhagic thrombocythemia |
| D47.4 |
Osteomyelofibrosis
Includes: Chronic idiopathic myelofibrosis Myelofibrosis (idiopathic) (with myeloid metaplasia) Myelosclerosis (megakaryocytic) with myeloid metaplasia Secondary myelofibrosis in myeloproliferative disease Excludes 1: acute myelofibrosis (C94.4-) |
| D47.Z1 | Post-transplant lymphoproliferative disorder (PTLD) |
| D47.Z2 |
Castleman disease
Excludes 2: Kaposi's sarcoma (C46.-) |
| D47.Z9 |
Other specified neoplasms of uncertain behavior of lymphoid, hematopoietic and related tissue
Includes: Histiocytic tumors of uncertain behavior |
| D47.9 |
Neoplasm of uncertain behavior oflymphoid, hematopoietic and related tissue, unspecified
Includes: Lymphoproliferative disease NOS |
| D48.0 |
Neoplasm of uncertain behavior ofbone and articular cartilage
Excludes 1: neoplasm of uncertain behavior of cartilage of ear (D48.1) neoplasm of uncertain behavior of cartilage of larynx (D38.0) neoplasm of uncertain behavior of cartilage of nose (D38.5) neoplasm of uncertain behavior of connective tissue of eyelid (D48.1) neoplasm of uncertain behavior of synovia (D48.1) |
| D48.1 |
Neoplasm of uncertain behavior ofconnective and other soft tissue
Includes: Neoplasm of uncertain behavior of connective tissue of ear Neoplasm of uncertain behavior of connective tissue of eyelid Stromal tumors of uncertain behavior of digestive system Excludes 1: neoplasm of uncertain behavior of articular cartilage (D48.0) neoplasm of uncertain behavior of cartilage of larynx (D38.0) neoplasm of uncertain behavior of cartilage of nose (D38.5) neoplasm of uncertain behavior of connective tissue of breast (D48.6-) |
| D48.2 |
Neoplasm of uncertain behavior ofperipheral nerves and autonomic nervous system
Excludes 1: neoplasm of uncertain behavior of peripheral nerves of orbit (D48.7) |
| D48.3 | Neoplasm of uncertain behavior ofretroperitoneum |
| D48.4 | Neoplasm of uncertain behavior ofperitoneum |
| D48.5 |
Neoplasm of uncertain behavior ofskin
Includes: Neoplasm of uncertain behavior of anal margin Neoplasm of uncertain behavior of anal skin Neoplasm of uncertain behavior of perianal skin Neoplasm of uncertain behavior of skin of breast Excludes 1: neoplasm of uncertain behavior of anus NOS (D37.8) neoplasm of uncertain behavior of skin of genital organs (D39.8, D40.8) neoplasm of uncertain behavior of vermilion border of lip (D37.0) |
| D48.60 | Neoplasm of uncertain behavior ofunspecified breast |
| D48.61 | Neoplasm of uncertain behavior ofright breast |
| D48.62 | Neoplasm of uncertain behavior ofleft breast |
| D48.7 |
Neoplasm of uncertain behavior ofother specified sites
Includes: Neoplasm of uncertain behavior of eye Neoplasm of uncertain behavior of heart Neoplasm of uncertain behavior of peripheral nerves of orbit Excludes 1: neoplasm of uncertain behavior of connective tissue (D48.1) neoplasm of uncertain behavior of skin of eyelid (D48.5) |
| D48.9 | Neoplasm of uncertain behavior, unspecified |
| D49.0 |
Neoplasm of unspecified behavior of digestive system
Excludes 1: neoplasm of unspecified behavior of margin of anus (D49.2) neoplasm of unspecified behavior of perianal skin (D49.2) neoplasm of unspecified behavior of skin of anus (D49.2) |
| D49.1 | Neoplasm of unspecified behavior of respiratory system |
| D49.2 |
Neoplasm of unspecified behavior of bone, soft tissue, and skin
Excludes 1: neoplasm of unspecified behavior of anal canal (D49.0) neoplasm of unspecified behavior of anus NOS (D49.0) neoplasm of unspecified behavior of bone marrow (D49.89) neoplasm of unspecified behavior of cartilage of larynx (D49.1) neoplasm of unspecified behavior of cartilage of nose (D49.1) neoplasm of unspecified behavior of connective tissue of breast (D49.3) neoplasm of unspecified behavior of skin of genital organs (D49.59) neoplasm of unspecified behavior of vermilion border of lip (D49.0) |
| D49.3 |
Neoplasm of unspecified behavior of breast
Excludes 1: neoplasm of unspecified behavior of skin of breast (D49.2) |
| D49.4 | Neoplasm of unspecified behavior of bladder |
| D49.511 | Neoplasm of unspecified behavior of right kidney |
| D49.512 | Neoplasm of unspecified behavior of left kidney |
| D49.519 | Neoplasm of unspecified behavior of unspecified kidney |
| D49.59 | Neoplasm of unspecified behavior of other genitourinary organ |
| D49.6 |
Neoplasm of unspecified behavior of brain
Excludes 1: neoplasm of unspecified behavior of cerebral meninges (D49.7) neoplasm of unspecified behavior of cranial nerves (D49.7) |
| D49.7 |
Neoplasm of unspecified behavior of endocrine glands and other parts of nervous system
Excludes 1: neoplasm of unspecified behavior of peripheral, sympathetic, and parasympathetic nerves and ganglia (D49.2) |
| D49.81 |
Neoplasm of unspecified behavior of retina and choroid
Includes: Dark area on retina Retinal freckle |
| D49.89 | Neoplasm of unspecified behavior of other specified sites |
| D49.9 | Neoplasm of unspecified behavior of unspecified site |
| D50.0 |
Iron deficiency anemia secondary to blood loss (chronic)
Includes: Posthemorrhagic anemia (chronic) Excludes 1: acute posthemorrhagic anemia (D62) congenital anemia from fetal blood loss (P61.3) |
| D50.1 |
Sideropenic dysphagia
Includes: Kelly-Paterson syndrome Plummer-Vinson syndrome |
| D50.8 |
Other iron deficiency anemias
Includes: Iron deficiency anemia due to inadequate dietary iron intake |
| D50.9 | Iron deficiency anemia, unspecified |
| D51.0 |
Vitamin B12 deficiency anemia dueto intrinsic factor deficiency
Includes: Addison anemia Biermer anemia Pernicious (congenital) anemia Congenital intrinsic factor deficiency |
| D51.1 |
Vitamin B12 deficiency anemia dueto selective vitamin B12 malabsorption with proteinuria
Includes: Imerslund (Gräsbeck) syndrome Megaloblastic hereditary anemia |
| D51.2 | Transcobalamin II deficiency |
| D51.3 |
Other dietary vitamin B12 deficiency anemia
Includes: Vegan anemia |
| D51.8 | Other vitamin B12 deficiency anemias |
| D51.9 | Vitamin B12 deficiency anemia, unspecified |
| D52.0 |
Dietary folate deficiency anemia
Includes: Nutritional megaloblastic anemia |
| D52.1 | Drug-induced folate deficiency anemia |
| D52.8 | Other folate deficiency anemias |
| D52.9 |
Folate deficiency anemia, unspecified
Includes: Folic acid deficiency anemia NOS |
| D53.0 |
Protein deficiency anemia
Includes: Amino-acid deficiency anemia Orotaciduric anemia Excludes 1: Lesch-Nyhan syndrome (E79.1) |
| D53.1 |
Other megaloblastic anemias, not elsewhere classified
Includes: Megaloblastic anemia NOS Excludes 1: Di Guglielmo's disease (C94.0) |
| D53.2 |
Scorbutic anemia
Excludes 1: scurvy (E54) |
| D53.8 |
Other specified nutritional anemias
Includes: Anemia associated with deficiency of copper Anemia associated with deficiency of molybdenum Anemia associated with deficiency of zinc Excludes 1: nutritional deficiencies without anemia, such as: copper deficiency NOS (E61.0) molybdenum deficiency NOS (E61.5) zinc deficiency NOS (E60) |
| D53.9 |
Nutritional anemia, unspecified
Includes: Simple chronic anemia Excludes 1: anemia NOS (D64.9) |
| D55.0 |
Anemia due to glucose-6-phosphatedehydrogenase [G6PD] deficiency
Includes: Favism G6PD deficiency anemia Excludes 1: glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia (D75.A) |
| D55.1 |
Anemia due to other disorders of glutathione metabolism
Includes: Anemia (due to) enzyme deficiencies, except G6PD, related to the hexose monophosphate [HMP] shunt pathway Anemia (due to) hemolytic nonspherocytic (hereditary), type I |
| D55.2 |
Anemia due to disorders of glycolytic enzymes
Includes: Hemolytic nonspherocytic (hereditary) anemia, type II Hexokinase deficiency anemia Pyruvate kinase [PK] deficiency anemia Triose-phosphate isomerase deficiency anemia Excludes 1: disorders of glycolysis not associated with anemia (E74.81-) |
| D55.3 | Anemia due to disorders of nucleotide metabolism |
| D55.8 | Other anemias due to enzyme disorders |
| D55.9 | Anemia due to enzyme disorder, unspecified |
| D56.0 |
Alpha thalassemia
Includes: Alpha thalassemia major Hemoglobin H Constant Spring Hemoglobin H disease Hydrops fetalis due to alpha thalassemia Severe alpha thalassemia Triple gene defect alpha thalassemia Excludes 1: alpha thalassemia trait or minor (D56.3) asymptomatic alpha thalassemia (D56.3) hydrops fetalis due to isoimmunization (P56.0) hydrops fetalis not due to immune hemolysis (P83.2) |
| D56.1 |
Beta thalassemia
Includes: Beta thalassemia major Cooley's anemia Homozygous beta thalassemia Severe beta thalassemia Thalassemia intermedia Thalassemia major Excludes 1: beta thalassemia minor (D56.3) beta thalassemia trait (D56.3) delta-beta thalassemia (D56.2) hemoglobin E-beta thalassemia (D56.5) sickle-cell beta thalassemia (D57.4-) |
| D56.2 |
Delta-beta thalassemia
Includes: Homozygous delta-beta thalassemia Excludes 1: delta-beta thalassemia minor (D56.3) delta-beta thalassemia trait (D56.3) |
| D56.3 |
Thalassemia minor
Includes: Alpha thalassemia minor Alpha thalassemia silent carrier Alpha thalassemia trait Beta thalassemia minor Beta thalassemia trait Delta-beta thalassemia minor Delta-beta thalassemia trait Thalassemia trait NOS Excludes 1: alpha thalassemia (D56.0) beta thalassemia (D56.1) delta-beta thalassemia (D56.2) hemoglobin E-beta thalassemia (D56.5) sickle-cell trait (D57.3) |
| D56.4 | Hereditary persistence of fetal hemoglobin [HPFH] |
| D56.5 |
Hemoglobin E-beta thalassemia
Excludes 1: beta thalassemia (D56.1) beta thalassemia minor (D56.3) beta thalassemia trait (D56.3) delta-beta thalassemia (D56.2) delta-beta thalassemia trait (D56.3) hemoglobin E disease (D58.2) other hemoglobinopathies (D58.2) sickle-cell beta thalassemia (D57.4-) |
| D56.8 |
Other thalassemias
Includes: Dominant thalassemia Hemoglobin C thalassemia Mixed thalassemia Thalassemia with other hemoglobinopathy Excludes 1: hemoglobin C disease (D58.2) hemoglobin E disease (D58.2) other hemoglobinopathies (D58.2) sickle-cell anemia (D57.-) sickle-cell thalassemia (D57.4) |
| D56.9 |
Thalassemia, unspecified
Includes: Mediterranean anemia (with other hemoglobinopathy) |
| D57.00 |
Hb-SS disease with crisis, unspecified
Includes: Hb-SS disease with (painful) crisis NOS Hb-SS disease with vasoocclusive pain NOS |
| D57.01 | Hb-SS disease with acute chest syndrome |
| D57.02 | Hb-SS disease with splenic sequestration |
| D57.03 | Hb-SS disease with cerebral vascular involvement |
| D57.09 | Hb-SS disease with crisis with other specified complication |
| D57.1 |
Sickle-cell disease without crisis
Includes: Hb-SS disease without crisis Sickle-cell anemia NOS Sickle-cell disease NOS Sickle-cell disorder NOS |
| D57.20 | Sickle-cell/Hb-C disease without crisis |
| D57.211 | Sickle-cell/Hb-C disease with acute chest syndrome |
| D57.212 | Sickle-cell/Hb-C disease with splenic sequestration |
| D57.213 | Sickle-cell/Hb-C disease with cerebral vascular involvement |
| D57.218 | Sickle-cell/Hb-C disease with crisis with other specified complication |
| D57.219 |
Sickle-cell/Hb-C disease with crisis, unspecified
Includes: Sickle-cell/Hb-C disease with crisis NOS Sickle-cell/Hb-C disease with vasoocclusive pain NOS |
| D57.3 |
Sickle-cell trait
Includes: Hb-S trait Heterozygous hemoglobin S |
| D57.40 |
Sickle-cell thalassemia without crisis
Includes: Microdrepanocytosis Sickle-cell thalassemia NOS |
| D57.411 | Sickle-cell thalassemia, unspecified, with acute chest syndrome |
| D57.412 | Sickle-cell thalassemia, unspecified, with splenic sequestration |
| D57.413 | Sickle-cell thalassemia, unspecified, with cerebral vascular involvement |
| D57.418 | Sickle-cell thalassemia, unspecified, with crisis with other specified complication |
| D57.419 |
Sickle-cell thalassemia, unspecified, with crisis
Includes: Sickle-cell thalassemia with (painful) crisis NOS Sickle-cell thalassemia with vasoocclusive pain |
| D57.42 |
Sickle-cell thalassemia beta zerowithout crisis
Includes: HbS-beta zero without crisis Sickle-cell beta zero without crisis |
| D57.431 |
Sickle-cell thalassemia beta zerowith acute chest syndrome
Includes: HbS-beta zero with acute chest syndrome Sickle-cell beta zero with acute chest syndrome |
| D57.432 |
Sickle-cell thalassemia beta zerowith splenic sequestration
Includes: HbS-beta zero with splenic sequestration Sickle-cell beta zero with splenic sequestration |
| D57.433 |
Sickle-cell thalassemia beta zerowith cerebral vascular involvement
Includes: HbS-beta zero with cerebral vascular involvement Sickle-cell beta zero with cerebral vascular involvement |
| D57.438 |
Sickle-cell thalassemia beta zerowith crisis with other specified complication
Includes: HbS-beta zero with other specified complication Sickle-cell beta zero with other specified complication |
| D57.439 |
Sickle-cell thalassemia beta zerowith crisis, unspecified
Includes: HbS-beta zero with other specified complication Sickle-cell beta zero with crisis unspecified Sickle-cell thalassemia beta zero with (painful) crisis NOS Sickle-cell thalassemia beta zero with vasoocclusive pain |
| D57.44 |
Sickle-cell thalassemia beta pluswithout crisis
Includes: HbS-beta plus without crisis Sickle-cell beta plus without crisis |
| D57.451 |
Sickle-cell thalassemia beta pluswith acute chest syndrome
Includes: HbS-beta plus with acute chest syndrome Sickle-cell beta plus with acute chest syndrome |
| D57.452 |
Sickle-cell thalassemia beta pluswith splenic sequestration
Includes: HbS-beta plus with splenic sequestration Sickle-cell beta plus with splenic sequestration |
| D57.453 |
Sickle-cell thalassemia beta pluswith cerebral vascular involvement
Includes: HbS-beta plus with cerebral vascular involvement Sickle-cell beta plus with cerebral vascular involvement |
| D57.458 |
Sickle-cell thalassemia beta pluswith crisis with other specified complication
Includes: HbS-beta plus with crisis with other specified complication Sickle-cell beta plus with crisis with other specified complication |
| D57.459 |
Sickle-cell thalassemia beta pluswith crisis, unspecified
Includes: HbS-beta plus with crisis with unspecified complication Sickle-cell beta plus with crisis with unspecified complication Sickle-cell thalassemia beta plus with (painful) crisis NOS Sickle-cell thalassemia beta plus with vasoocclusive pain |
| D57.80 | Other sickle-cell disorders without crisis |
| D57.811 | Other sickle-cell disorders with acute chest syndrome |
| D57.812 | Other sickle-cell disorders with splenic sequestration |
| D57.813 | Other sickle-cell disorders with cerebral vascular involvement |
| D57.818 | Other sickle-cell disorders with crisis with other specified complication |
| D57.819 |
Other sickle-cell disorders with crisis, unspecified
Includes: Other sickle-cell disorders with crisis NOS Other sickle-cell disorders with vasooclusive pain NOS |
| D58.0 |
Hereditary spherocytosis
Includes: Acholuric (familial) jaundice Congenital (spherocytic) hemolytic icterus Minkowski-Chauffard syndrome |
| D58.1 |
Hereditary elliptocytosis
Includes: Elliptocytosis (congenital) Ovalocytosis (congenital) (hereditary) |
| D58.2 |
Other hemoglobinopathies
Includes: Abnormal hemoglobin NOS Congenital Heinz body anemia Hb-C disease Hb-D disease Hb-E disease Hemoglobinopathy NOS Unstable hemoglobin hemolytic disease Excludes 1: familial polycythemia (D75.0) Hb-M disease (D74.0) hemoglobin E-beta thalassemia (D56.5) hereditary persistence of fetal hemoglobin [HPFH] (D56.4) high-altitude polycythemia (D75.1) methemoglobinemia (D74.-) other hemoglobinopathies with thalassemia (D56.8) |
| D58.8 |
Other specified hereditary hemolytic anemias
Includes: Stomatocytosis |
| D58.9 | Hereditary hemolytic anemia, unspecified |
| D59.0 | Drug-induced autoimmune hemolyticanemia |
| D59.10 | Autoimmune hemolytic anemia, unspecified |
| D59.11 |
Warm autoimmune hemolytic anemia
Includes: Warm type (primary) (secondary) (symptomatic) autoimmune hemolytic anemia Warm type autoimmune hemolytic disease |
| D59.12 |
Cold autoimmune hemolytic anemia
Includes: Chronic cold hemagglutinin disease Cold agglutinin disease Cold agglutinin hemoglobinuria Cold type (primary) (secondary) (symptomatic) autoimmune hemolytic anemia Cold type autoimmune hemolytic disease |
| D59.13 |
Mixed type autoimmune hemolytic anemia
Includes: Mixed type autoimmune hemolytic disease Mixed type, cold and warm, (primary) (secondary) (symptomatic) autoimmune hemolytic anemia |
| D59.19 | Other autoimmune hemolytic anemia |
| D59.2 |
Drug-induced nonautoimmune hemolytic anemia
Includes: Drug-induced enzyme deficiency anemia |
| D59.3 | Hemolytic-uremic syndrome |
| D59.4 |
Other nonautoimmune hemolytic anemias
Includes: Mechanical hemolytic anemia Microangiopathic hemolytic anemia Toxic hemolytic anemia |
| D59.5 |
Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
Excludes 1: hemoglobinuria NOS (R82.3) |
| D59.6 |
Hemoglobinuria due to hemolysis from other external causes
Includes: Hemoglobinuria from exertion March hemoglobinuria Paroxysmal cold hemoglobinuria Excludes 1: hemoglobinuria NOS (R82.3) |
| D59.8 | Other acquired hemolytic anemias |
| D59.9 |
Acquired hemolytic anemia, unspecified
Includes: Idiopathic hemolytic anemia, chronic |
| D60.0 | Chronic acquired pure red cell aplasia |
| D60.1 | Transient acquired pure red cell aplasia |
| D60.8 | Other acquired pure red cell aplasias |
| D60.9 | Acquired pure red cell aplasia, unspecified |
| D61.01 |
Constitutional (pure) red blood cell aplasia
Includes: Blackfan-Diamond syndrome Congenital (pure) red cell aplasia Familial hypoplastic anemia Primary (pure) red cell aplasia Red cell (pure) aplasia of infants Excludes 1: acquired red cell aplasia (D60.9) |
| D61.09 |
Other constitutional aplastic anemia
Includes: Fanconi's anemia Pancytopenia with malformations |
| D61.1 | Drug-induced aplastic anemia |
| D61.2 | Aplastic anemia due to other external agents |
| D61.3 | Idiopathic aplastic anemia |
| D61.810 |
Antineoplastic chemotherapy induced pancytopenia
Excludes 2: aplastic anemia due to antineoplastic chemotherapy (D61.1) |
| D61.811 |
Other drug-induced pancytopenia
Excludes 2: aplastic anemia due to drugs (D61.1) |
| D61.818 | Other pancytopenia |
| D61.82 |
Myelophthisis
Includes: Leukoerythroblastic anemia Myelophthisic anemia Panmyelophthisis Excludes 1: idiopathic myelofibrosis (D47.1) myelofibrosis NOS (D75.81) myelofibrosis with myeloid metaplasia (D47.4) primary myelofibrosis (D47.1) secondary myelofibrosis (D75.81) |
| D61.89 | Other specified aplastic anemias and other bone marrow failure syndromes |
| D61.9 |
Aplastic anemia, unspecified
Includes: Hypoplastic anemia NOS Medullary hypoplasia |
| D62 |
Acute posthemorrhagic anemia
Excludes 1: anemia due to chronic blood loss (D50.0) blood loss anemia NOS (D50.0) congenital anemia from fetal blood loss (P61.3) |
| D63.0 |
Anemia in neoplastic disease
Excludes 1: aplastic anemia due to antineoplastic chemotherapy (D61.1) Excludes 2: anemia due to antineoplastic chemotherapy (D64.81) |
| D63.1 |
Anemia in chronic kidney disease
Includes: Erythropoietin resistant anemia (EPO resistant anemia) |
| D63.8 | Anemia in other chronic diseases classified elsewhere |
| D64.0 |
Hereditary sideroblastic anemia
Includes: Sex-linked hypochromic sideroblastic anemia |
| D64.1 | Secondary sideroblastic anemia dueto disease |
| D64.2 | Secondary sideroblastic anemia dueto drugs and toxins |
| D64.3 |
Other sideroblastic anemias
Includes: Sideroblastic anemia NOS Pyridoxine-responsive sideroblastic anemia NEC |
| D64.4 |
Congenital dyserythropoietic anemia
Includes: Dyshematopoietic anemia (congenital) Excludes 1: Blackfan-Diamond syndrome (D61.01) Di Guglielmo's disease (C94.0) |
| D64.81 |
Anemia due to antineoplastic chemotherapy
Includes: Antineoplastic chemotherapy induced anemia Excludes 1: aplastic anemia due to antineoplastic chemotherapy (D61.1) Excludes 2: anemia in neoplastic disease (D63.0) |
| D64.89 |
Other specified anemias
Includes: Infantile pseudoleukemia |
| D64.9 | Anemia, unspecified |
| D65 |
Disseminated intravascular coagulation [defibrination syndrome]
Includes: Afibrinogenemia, acquired Consumption coagulopathy Diffuse or disseminated intravascular coagulation [DIC] Fibrinolytic hemorrhage, acquired Fibrinolytic purpura Purpura fulminans Excludes 1: disseminated intravascular coagulation (complicating): abortion or ectopic or molar pregnancy (O00-O07, O08.1) in newborn (P60) pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3) |
| D66 |
Hereditary factor VIII deficiency
Includes: Classical hemophilia Deficiency factor VIII (with functional defect) Hemophilia NOS Hemophilia A Excludes 1: factor VIII deficiency with vascular defect (D68.0) |
| D67 |
Hereditary factor IX deficiency
Includes: Christmas disease Factor IX deficiency (with functional defect) Hemophilia B Plasma thromboplastin component [PTC] deficiency |
| D68.0 |
Von Willebrand's disease
Includes: Angiohemophilia Factor VIII deficiency with vascular defect Vascular hemophilia Excludes 1: capillary fragility (hereditary) (D69.8) factor VIII deficiency NOS (D66) factor VIII deficiency with functional defect (D66) |
| D68.1 |
Hereditary factor XI deficiency
Includes: Hemophilia C Plasma thromboplastin antecedent [PTA] deficiency Rosenthal's disease |
| D68.2 |
Hereditary deficiency of other clotting factors
Includes: AC globulin deficiency Congenital afibrinogenemia Deficiency of factor I [fibrinogen] Deficiency of factor II [prothrombin] Deficiency of factor V [labile] Deficiency of factor VII [stable] Deficiency of factor X [Stuart-Prower] Deficiency of factor XII [Hageman] Deficiency of factor XIII [fibrin stabilizing] Dysfibrinogenemia (congenital) Hypoproconvertinemia Owren's disease Proaccelerin deficiency |
| D68.311 |
Acquired hemophilia
Includes: Autoimmune hemophilia Autoimmune inhibitors to clotting factors Secondary hemophilia |
| D68.312 |
Antiphospholipid antibody with hemorrhagic disorder
Includes: Lupus anticoagulant (LAC) with hemorrhagic disorder Systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder Excludes 1: antiphospholipid antibody, finding without diagnosis (R76.0) antiphospholipid antibody syndrome (D68.61) antiphospholipid antibody with hypercoagulable state (D68.61) lupus anticoagulant (LAC) finding without diagnosis (R76.0) lupus anticoagulant (LAC) with hypercoagulable state (D68.62) systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0) systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.62) |
| D68.318 |
Other hemorrhagic disorder due tointrinsic circulating anticoagulants, antibodies, or inhibitors
Includes: Antithromboplastinemia Antithromboplastinogenemia Hemorrhagic disorder due to intrinsic increase in antithrombin Hemorrhagic disorder due to intrinsic increase in anti-VIIIa Hemorrhagic disorder due to intrinsic increase in anti-IXa Hemorrhagic disorder due to intrinsic increase in anti-XIa |
| D68.32 |
Hemorrhagic disorder due to extrinsic circulating anticoagulants
Includes: Drug-induced hemorrhagic disorder Hemorrhagic disorder due to increase in anti-IIa Hemorrhagic disorder due to increase in anti-Xa Hyperheparinemia |
| D68.4 |
Acquired coagulation factor deficiency
Includes: Deficiency of coagulation factor due to liver disease Deficiency of coagulation factor due to vitamin K deficiency Excludes 1: vitamin K deficiency of newborn (P53) |
| D68.51 |
Activated protein C resistance
Includes: Factor V Leiden mutation |
| D68.52 | Prothrombin gene mutation |
| D68.59 |
Other primary thrombophilia
Includes: Antithrombin III deficiency Hypercoagulable state NOS Primary hypercoagulable state NEC Primary thrombophilia NEC Protein C deficiency Protein S deficiency Thrombophilia NOS |
| D68.61 |
Antiphospholipid syndrome
Includes: Anticardiolipin syndrome Antiphospholipid antibody syndrome Excludes 1: anti-phospholipid antibody, finding without diagnosis (R76.0) anti-phospholipid antibody with hemorrhagic disorder (D68.312) lupus anticoagulant syndrome (D68.62) |
| D68.62 |
Lupus anticoagulant syndrome
Includes: Lupus anticoagulant Presence of systemic lupus erythematosus [SLE] inhibitor Excludes 1: anticardiolipin syndrome (D68.61) antiphospholipid syndrome (D68.61) lupus anticoagulant (LAC) finding without diagnosis (R76.0) lupus anticoagulant (LAC) with hemorrhagic disorder (D68.312) |
| D68.69 |
Other thrombophilia
Includes: Hypercoagulable states NEC Secondary hypercoagulable state NOS |
| D68.8 |
Other specified coagulation defects
Excludes 1: hemorrhagic disease of newborn (P53) |
| D68.9 | Coagulation defect, unspecified |
| D69.0 |
Allergic purpura
Includes: Allergic vasculitis Nonthrombocytopenic hemorrhagic purpura Nonthrombocytopenic idiopathic purpura Purpura anaphylactoid Purpura Henoch(-Schönlein) Purpura rheumatica Vascular purpura Excludes 1: thrombocytopenic hemorrhagic purpura (D69.3) |
| D69.1 |
Qualitative platelet defects
Includes: Bernard-Soulier [giant platelet] syndrome Glanzmann's disease Grey platelet syndrome Thromboasthenia (hemorrhagic) (hereditary) Thrombocytopathy Excludes 1: von Willebrand's disease (D68.0) |
| D69.2 |
Other nonthrombocytopenic purpura
Includes: Purpura NOS Purpura simplex Senile purpura |
| D69.3 |
Immune thrombocytopenic purpura
Includes: Hemorrhagic (thrombocytopenic) purpura Idiopathic thrombocytopenic purpura Tidal platelet dysgenesis |
| D69.41 | Evans syndrome |
| D69.42 |
Congenital and hereditary thrombocytopenia purpura
Includes: Congenital thrombocytopenia Hereditary thrombocytopenia |
| D69.49 |
Other primary thrombocytopenia
Includes: Megakaryocytic hypoplasia Primary thrombocytopenia NOS |
| D69.51 |
Posttransfusion purpura
Includes: Posttransfusion purpura from whole blood (fresh) or blood products PTP |
| D69.59 | Other secondary thrombocytopenia |
| D69.6 | Thrombocytopenia, unspecified |
| D69.8 |
Other specified hemorrhagic conditions
Includes: Capillary fragility (hereditary) Vascular pseudohemophilia |
| D69.9 | Hemorrhagic condition, unspecified |
| D70.0 |
Congenital agranulocytosis
Includes: Congenital neutropenia Infantile genetic agranulocytosis Kostmann's disease |
| D70.1 | Agranulocytosis secondary to cancer chemotherapy |
| D70.2 | Other drug-induced agranulocytosis |
| D70.3 | Neutropenia due to infection |
| D70.4 |
Cyclic neutropenia
Includes: Cyclic hematopoiesis Periodic neutropenia |
| D70.8 | Other neutropenia |
| D70.9 | Neutropenia, unspecified |
| D71 |
Functional disorders of polymorphonuclear neutrophils
Includes: Cell membrane receptor complex [CR3] defect Chronic (childhood) granulomatous disease Congenital dysphagocytosis Progressive septic granulomatosis |
| D72.0 |
Genetic anomalies of leukocytes
Includes: Alder (granulation) (granulocyte) anomaly Alder syndrome Hereditary leukocytic hypersegmentation Hereditary leukocytic hyposegmentation Hereditary leukomelanopathy May-Hegglin (granulation) (granulocyte) anomaly May-Hegglin syndrome Pelger-Huët (granulation) (granulocyte) anomaly Pelger-Huët syndrome Excludes 1: Chédiak (-Steinbrinck)-Higashi syndrome (E70.330) |
| D72.10 | Eosinophilia, unspecified |
| D72.110 | Idiopathic hypereosinophilic syndrome [IHES] |
| D72.111 |
Lymphocytic Variant Hypereosinophilic Syndrome [LHES]
Includes: Lymphocyte variant hypereosinophilia |
| D72.118 |
Other hypereosinophilic syndrome
Includes: Episodic angioedema with eosinophilia Gleich's syndrome |
| D72.119 | Hypereosinophilic syndrome [HES],unspecified |
| D72.12 |
Drug rash with eosinophilia and systemic symptoms syndrome
Includes: DRESS syndrome |
| D72.18 | Eosinophilia in diseases classified elsewhere |
| D72.19 |
Other eosinophilia
Includes: Familial eosinophilia Hereditary eosinophilia |
| D72.810 |
Lymphocytopenia
Includes: Decreased lymphocytes |
| D72.818 |
Other decreased white blood cell count
Includes: Basophilic leukopenia Eosinophilic leukopenia Monocytopenia Other decreased leukocytes Plasmacytopenia |
| D72.819 |
Decreased white blood cell count,unspecified
Includes: Decreased leukocytes, unspecified Leukocytopenia, unspecified Leukopenia Excludes 1: malignant leukopenia (D70.9) |
| D72.820 |
Lymphocytosis (symptomatic)
Includes: Elevated lymphocytes |
| D72.821 |
Monocytosis (symptomatic)
Excludes 1: infectious mononucleosis (B27.-) |
| D72.822 | Plasmacytosis |
| D72.823 |
Leukemoid reaction
Includes: Basophilic leukemoid reaction Leukemoid reaction NOS Lymphocytic leukemoid reaction Monocytic leukemoid reaction Myelocytic leukemoid reaction Neutrophilic leukemoid reaction |
| D72.824 | Basophilia |
| D72.825 |
Bandemia
Includes: Bandemia without diagnosis of specific infection Excludes 1: confirmed infection - code to infection leukemia (C91.-, C92.-, C93.-, C94.-, C95.-) |
| D72.828 | Other elevated white blood cell count |
| D72.829 |
Elevated white blood cell count, unspecified
Includes: Elevated leukocytes, unspecified Leukocytosis, unspecified |
| D72.89 |
Other specified disorders of whiteblood cells
Includes: Abnormality of white blood cells NEC |
| D72.9 |
Disorder of white blood cells, unspecified
Includes: Abnormal leukocyte differential NOS |
| D73.0 |
Hyposplenism
Includes: Atrophy of spleen Excludes 1: asplenia (congenital) (Q89.01) postsurgical absence of spleen (Z90.81) |
| D73.1 |
Hypersplenism
Excludes 1: neutropenic splenomegaly (D73.81) primary splenic neutropenia (D73.81) splenitis, splenomegaly in late syphilis (A52.79) splenitis, splenomegaly in tuberculosis (A18.85) splenomegaly NOS (R16.1) splenomegaly congenital (Q89.0) |
| D73.2 | Chronic congestive splenomegaly |
| D73.3 | Abscess of spleen |
| D73.4 | Cyst of spleen |
| D73.5 |
Infarction of spleen
Includes: Splenic rupture, nontraumatic Torsion of spleen Excludes 1: rupture of spleen due to Plasmodium vivax malaria (B51.0) traumatic rupture of spleen (S36.03-) |
| D73.81 |
Neutropenic splenomegaly
Includes: Werner-Schultz disease |
| D73.89 |
Other diseases of spleen
Includes: Fibrosis of spleen NOS Perisplenitis Splenitis NOS |
| D73.9 | Disease of spleen, unspecified |
| D74.0 |
Congenital methemoglobinemia
Includes: Congenital NADH-methemoglobin reductase deficiency Hemoglobin-M [Hb-M] disease Methemoglobinemia, hereditary |
| D74.8 |
Other methemoglobinemias
Includes: Acquired methemoglobinemia (with sulfhemoglobinemia) Toxic methemoglobinemia |
| D74.9 | Methemoglobinemia, unspecified |
| D75.0 |
Familial erythrocytosis
Includes: Benign polycythemia Familial polycythemia Excludes 1: hereditary ovalocytosis (D58.1) |
| D75.1 |
Secondary polycythemia
Includes: Acquired polycythemia Emotional polycythemia Erythrocytosis NOS Hypoxemic polycythemia Nephrogenous polycythemia Polycythemia due to erythropoietin Polycythemia due to fall in plasma volume Polycythemia due to high altitude Polycythemia due to stress Polycythemia NOS Relative polycythemia Excludes 1: polycythemia neonatorum (P61.1) polycythemia vera (D45) |
| D75.81 |
Myelofibrosis
Includes: Myelofibrosis NOS Secondary myelofibrosis NOS Excludes 1: acute myelofibrosis (C94.4-) idiopathic myelofibrosis (D47.1) leukoerythroblastic anemia (D61.82) myelofibrosis with myeloid metaplasia (D47.4) myelophthisic anemia (D61.82) myelophthisis (D61.82) primary myelofibrosis (D47.1) |
| D75.82 | Heparin induced thrombocytopenia (HIT) |
| D75.89 | Other specified diseases of bloodand blood-forming organs |
| D75.9 | Disease of blood and blood-formingorgans, unspecified |
| D75.A |
Glucose-6-phosphate dehydrogenase(G6PD) deficiency without anemia
Excludes 1: glucose-6-phosphate dehydrogenase (G6PD) deficiency with anemia (D55.0) |
| D76.1 |
Hemophagocytic lymphohistiocytosis
Includes: Familial hemophagocytic reticulosis Histiocytoses of mononuclear phagocytes |
| D76.2 | #NAME? |
| D76.3 |
Other histiocytosis syndromes
Includes: Reticulohistiocytoma (giant-cell) Sinus histiocytosis with massive lymphadenopathy Xanthogranuloma |
| D77 |
#NAME?
Excludes 1: rupture of spleen due to Plasmodium vivax malaria (B51.0) splenitis, splenomegaly in late syphilis (A52.79) splenitis, splenomegaly in tuberculosis (A18.85) |
| D78.01 | Intraoperative hemorrhage and hematoma of the spleen complicating a procedure on the spleen |
| D78.02 | Intraoperative hemorrhage and hematoma of the spleen complicating other procedure |
| D78.11 | Accidental puncture and lacerationof the spleen during a procedure on the spleen |
| D78.12 | Accidental puncture and lacerationof the spleen during other procedure |
| D78.21 | Postprocedural hemorrhage of the spleen following a procedure on the spleen |
| D78.22 | Postprocedural hemorrhage of the spleen following other procedure |
| D78.31 | Postprocedural hematoma of the spleen following a procedure on the spleen |
| D78.32 | Postprocedural hematoma of the spleen following other procedure |
| D78.33 | Postprocedural seroma of the spleen following a procedure on the spleen |
| D78.34 | Postprocedural seroma of the spleen following other procedure |
| D78.81 | Other intraoperative complicationsof the spleen |
| D78.89 | Other postprocedural complicationsof the spleen |
| D80.0 |
Hereditary hypogammaglobulinemia
Includes: Autosomal recessive agammaglobulinemia (Swiss type) X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency) |
| D80.1 |
Nonfamilial hypogammaglobulinemia
Includes: Agammaglobulinemia with immunoglobulin-bearing B-lymphocytes Common variable agammaglobulinemia [CVAgamma] Hypogammaglobulinemia NOS |
| D80.2 | Selective deficiency of immunoglobulin A [IgA] |
| D80.3 | Selective deficiency of immunoglobulin G [IgG] subclasses |
| D80.4 | Selective deficiency of immunoglobulin M [IgM] |
| D80.5 | Immunodeficiency with increased immunoglobulin M [IgM] |
| D80.6 | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia |
| D80.7 | Transient hypogammaglobulinemia ofinfancy |
| D80.8 |
Other immunodeficiencies with predominantly antibody defects
Includes: Kappa light chain deficiency |
| D80.9 | Immunodeficiency with predominantly antibody defects, unspecified |
| D81.0 | Severe combined immunodeficiency [SCID] with reticular dysgenesis |
| D81.1 | Severe combined immunodeficiency [SCID] with low T- and B-cell numbers |
| D81.2 | Severe combined immunodeficiency [SCID] with low or normal B-cell numbers |
| D81.30 |
Adenosine deaminase deficiency, unspecified
Includes: ADA deficiency NOS |
| D81.31 |
Severe combined immunodeficiency due to adenosine deaminase deficiency
Includes: ADA deficiency with SCID Adenosine deaminase [ADA] deficiency with severe combined immunodeficiency |
| D81.32 |
Adenosine deaminase 2 deficiency
Includes: ADA2 deficiency Adenosine deaminase deficiency type 2 |
| D81.39 |
Other adenosine deaminase deficiency
Includes: Adenosine deaminase [ADA] deficiency type 1, NOS Adenosine deaminase [ADA] deficiency type 1, without SCID Adenosine deaminase [ADA] deficiency type 1, without severe combined immunodeficiency Partial ADA deficiency (type 1) Partial adenosine deaminase deficiency (type 1) |
| D81.4 | Nezelof's syndrome |
| D81.5 | Purine nucleoside phosphorylase [PNP] deficiency |
| D81.6 |
Major histocompatibility complex class I deficiency
Includes: Bare lymphocyte syndrome |
| D81.7 | Major histocompatibility complex class II deficiency |
| D81.810 | Biotinidase deficiency |
| D81.818 |
Other biotin-dependent carboxylasedeficiency
Includes: Holocarboxylase synthetase deficiency Other multiple carboxylase deficiency |
| D81.819 |
Biotin-dependent carboxylase deficiency, unspecified
Includes: Multiple carboxylase deficiency, unspecified |
| D81.89 | Other combined immunodeficiencies |
| D81.9 |
Combined immunodeficiency, unspecified
Includes: Severe combined immunodeficiency disorder [SCID] NOS |
| D82.0 |
Wiskott-Aldrich syndrome
Includes: Immunodeficiency with thrombocytopenia and eczema |
| D82.1 |
Di George's syndrome
Includes: Pharyngeal pouch syndrome Thymic alymphoplasia Thymic aplasia or hypoplasia with immunodeficiency |
| D82.2 | Immunodeficiency with short-limbedstature |
| D82.3 |
Immunodeficiency following hereditary defective response to Epstein-Barr virus
Includes: X-linked lymphoproliferative disease |
| D82.4 | Hyperimmunoglobulin E [IgE] syndrome |
| D82.8 | Immunodeficiency associated with other specified major defects |
| D82.9 | Immunodeficiency associated with major defect, unspecified |
| D83.0 | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
| D83.1 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
| D83.2 | Common variable immunodeficiency with autoantibodies to B- or T-cells |
| D83.8 | Other common variable immunodeficiencies |
| D83.9 | Common variable immunodeficiency,unspecified |
| D84.0 | Lymphocyte function antigen-1 [LFA-1] defect |
| D84.1 |
Defects in the complement system
Includes: C1 esterase inhibitor [C1-INH] deficiency |
| D84.81 |
Immunodeficiency due to conditionsclassified elsewhere
Excludes 1: certain disorders involving the immune mechanism (D80-D83, D84.0, D84.1, D84.9) human immunodeficiency virus [HIV] disease (B20) |
| D84.821 |
Immunodeficiency due to drugs
Includes: Immunodeficiency due to (current or past) medication |
| D84.822 | Immunodeficiency due to external causes |
| D84.89 | Other immunodeficiencies |
| D84.9 |
Immunodeficiency, unspecified
Includes: Immunocompromised NOS Immunodeficient NOS Immunosuppressed NOS |
| D86.0 | Sarcoidosis of lung |
| D86.1 | Sarcoidosis of lymph nodes |
| D86.2 | Sarcoidosis of lung with sarcoidosis of lymph nodes |
| D86.3 | Sarcoidosis of skin |
| D86.81 | Sarcoid meningitis |
| D86.82 | Multiple cranial nerve palsies insarcoidosis |
| D86.83 | Sarcoid iridocyclitis |
| D86.84 |
Sarcoid pyelonephritis
Includes: Tubulo-interstitial nephropathy in sarcoidosis |
| D86.85 | Sarcoid myocarditis |
| D86.86 |
Sarcoid arthropathy
Includes: Polyarthritis in sarcoidosis |
| D86.87 | Sarcoid myositis |
| D86.89 |
Sarcoidosis of other sites
Includes: Hepatic granuloma Uveoparotid fever [Heerfordt] |
| D86.9 | Sarcoidosis, unspecified |
| D89.0 |
Polyclonal hypergammaglobulinemia
Includes: Benign hypergammaglobulinemic purpura Polyclonal gammopathy NOS |
| D89.1 |
Cryoglobulinemia
Includes: Cryoglobulinemic purpura Cryoglobulinemic vasculitis Essential cryoglobulinemia Idiopathic cryoglobulinemia Mixed cryoglobulinemia Primary cryoglobulinemia Secondary cryoglobulinemia |
| D89.2 | Hypergammaglobulinemia, unspecified |
| D89.3 |
Immune reconstitution syndrome
Includes: Immune reconstitution inflammatory syndrome [IRIS] |
| D89.40 |
Mast cell activation, unspecified
Includes: Mast cell activation disorder, unspecified Mast cell activation syndrome, NOS |
| D89.41 | Monoclonal mast cell activation syndrome |
| D89.42 | Idiopathic mast cell activation syndrome |
| D89.43 |
Secondary mast cell activation
Includes: Secondary mast cell activation syndrome |
| D89.49 |
Other mast cell activation disorder
Includes: Other mast cell activation syndrome |
| D89.810 | Acute graft-versus-host disease |
| D89.811 | Chronic graft-versus-host disease |
| D89.812 | Acute on chronic graft-versus-hostdisease |
| D89.813 | Graft-versus-host disease, unspecified |
| D89.82 | Autoimmune lymphoproliferative syndrome [ALPS] |
| D89.831 | Cytokine release syndrome, grade 1 |
| D89.832 | Cytokine release syndrome, grade 2 |
| D89.833 | Cytokine release syndrome, grade 3 |
| D89.834 | Cytokine release syndrome, grade 4 |
| D89.835 | Cytokine release syndrome, grade 5 |
| D89.839 | Cytokine release syndrome, grade unspecified |
| D89.89 |
Other specified disorders involving the immune mechanism, not elsewhere classified
Excludes 1: human immunodeficiency virus disease (B20) |
| D89.9 |
Disorder involving the immune mechanism, unspecified
Includes: Immune disease NOS |
| E00.0 |
Congenital iodine-deficiency syndrome, neurological type
Includes: Endemic cretinism, neurological type |
| E00.1 |
Congenital iodine-deficiency syndrome, myxedematous type
Includes: Endemic hypothyroid cretinism Endemic cretinism, myxedematous type |
| E00.2 |
Congenital iodine-deficiency syndrome, mixed type
Includes: Endemic cretinism, mixed type |
| E00.9 |
Congenital iodine-deficiency syndrome, unspecified
Includes: Congenital iodine-deficiency hypothyroidism NOS Endemic cretinism NOS |
| E01.0 | Iodine-deficiency related diffuse(endemic) goiter |
| E01.1 |
Iodine-deficiency related multinodular (endemic) goiter
Includes: Iodine-deficiency related nodular goiter |
| E01.2 |
Iodine-deficiency related (endemic) goiter, unspecified
Includes: Endemic goiter NOS |
| E01.8 |
Other iodine-deficiency related thyroid disorders and allied conditions
Includes: Acquired iodine-deficiency hypothyroidism NOS |
| E02 | Subclinical iodine-deficiency hypothyroidism |
| E03.0 |
Congenital hypothyroidism with diffuse goiter
Includes: Congenital parenchymatous goiter (nontoxic) Congenital goiter (nontoxic) NOS Excludes 1: transitory congenital goiter with normal function (P72.0) |
| E03.1 |
Congenital hypothyroidism withoutgoiter
Includes: Aplasia of thyroid (with myxedema) Congenital atrophy of thyroid Congenital hypothyroidism NOS |
| E03.2 | Hypothyroidism due to medicamentsand other exogenous substances |
| E03.3 | Postinfectious hypothyroidism |
| E03.4 |
Atrophy of thyroid (acquired)
Excludes 1: congenital atrophy of thyroid (E03.1) |
| E03.5 | Myxedema coma |
| E03.8 | Other specified hypothyroidism |
| E03.9 |
Hypothyroidism, unspecified
Includes: Myxedema NOS |
| E04.0 |
Nontoxic diffuse goiter
Includes: Diffuse (colloid) nontoxic goiter Simple nontoxic goiter |
| E04.1 |
Nontoxic single thyroid nodule
Includes: Colloid nodule (cystic) (thyroid) Nontoxic uninodular goiter Thyroid (cystic) nodule NOS |
| E04.2 |
Nontoxic multinodular goiter
Includes: Cystic goiter NOS Multinodular (cystic) goiter NOS |
| E04.8 | Other specified nontoxic goiter |
| E04.9 |
Nontoxic goiter, unspecified
Includes: Goiter NOS Nodular goiter (nontoxic) NOS |
| E05.00 | Thyrotoxicosis with diffuse goiterwithout thyrotoxic crisis or storm |
| E05.01 | Thyrotoxicosis with diffuse goiterwith thyrotoxic crisis or storm |
| E05.10 | Thyrotoxicosis with toxic single thyroid nodule without thyrotoxic crisis or storm |
| E05.11 | Thyrotoxicosis with toxic single thyroid nodule with thyrotoxic crisis or storm |
| E05.20 | Thyrotoxicosis with toxic multinodular goiter without thyrotoxic crisis or storm |
| E05.21 | Thyrotoxicosis with toxic multinodular goiter with thyrotoxic crisis or storm |
| E05.30 | Thyrotoxicosis from ectopic thyroid tissue without thyrotoxic crisis or storm |