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Medical Billing Code Search

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75105 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 specified parts of central nervous system
D33.9 Benign neoplasm of central nervous system, 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 and other paraganglia
Includes: Benign tumor of glomus jugulare
D35.7 Benign neoplasm of other specified endocrine 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 specified sites
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 of lip
Includes: Neoplasm of uncertain behavior of vermilion border of lip
D37.02 Neoplasm of uncertain behavior of tongue
D37.030 Neoplasm of uncertain behavior of the parotid salivary glands
D37.031 Neoplasm of uncertain behavior of the sublingual salivary glands
D37.032 Neoplasm of uncertain behavior of the submandibular salivary glands
D37.039 Neoplasm of uncertain behavior of the major salivary glands, unspecified
D37.04 Neoplasm of uncertain behavior of the 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 of pharynx
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 of other specified sites of the oral cavity
D37.1 Neoplasm of uncertain behavior of stomach
D37.2 Neoplasm of uncertain behavior of small intestine
D37.3 Neoplasm of uncertain behavior of appendix
D37.4 Neoplasm of uncertain behavior of colon
D37.5 Neoplasm of uncertain behavior of rectum
Includes: Neoplasm of uncertain behavior of rectosigmoid junction
D37.6 Neoplasm of uncertain behavior of liver, gallbladder and bile ducts
Includes: Neoplasm of uncertain behavior of ampulla of Vater
D37.8 Neoplasm of uncertain behavior of other 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 of digestive organ, unspecified
D38.0 Neoplasm of uncertain behavior of larynx
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 of trachea, bronchus and lung
D38.2 Neoplasm of uncertain behavior of pleura
D38.3 Neoplasm of uncertain behavior of mediastinum
D38.4 Neoplasm of uncertain behavior of thymus
D38.5 Neoplasm of uncertain behavior of other 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 of respiratory organ, unspecified
D39.0 Neoplasm of uncertain behavior of uterus
D39.10 Neoplasm of uncertain behavior of unspecified ovary
D39.11 Neoplasm of uncertain behavior of right ovary
D39.12 Neoplasm of uncertain behavior of left ovary
D39.2 Neoplasm of uncertain behavior of placenta
Includes: Chorioadenoma destruens Invasive hydatidiform mole Malignant hydatidiform mole
Excludes 1: hydatidiform mole NOS (O01.9)
D39.8 Neoplasm of uncertain behavior of other specified female genital organs
Includes: Neoplasm of uncertain behavior of skin of female genital organs
D39.9 Neoplasm of uncertain behavior of female genital organ, unspecified
D40.0 Neoplasm of uncertain behavior of prostate
D40.10 Neoplasm of uncertain behavior of unspecified testis
D40.11 Neoplasm of uncertain behavior of right testis
D40.12 Neoplasm of uncertain behavior of left testis
D40.8 Neoplasm of uncertain behavior of other specified male genital organs
Includes: Neoplasm of uncertain behavior of skin of male genital organs
D40.9 Neoplasm of uncertain behavior of male genital organ, unspecified
D41.00 Neoplasm of uncertain behavior of unspecified kidney
D41.01 Neoplasm of uncertain behavior of right kidney
D41.02 Neoplasm of uncertain behavior of left kidney
D41.10 Neoplasm of uncertain behavior of unspecified renal pelvis
D41.11 Neoplasm of uncertain behavior of right renal pelvis
D41.12 Neoplasm of uncertain behavior of left renal pelvis
D41.20 Neoplasm of uncertain behavior of unspecified ureter
D41.21 Neoplasm of uncertain behavior of right ureter
D41.22 Neoplasm of uncertain behavior of left ureter
D41.3 Neoplasm of uncertain behavior of urethra
D41.4 Neoplasm of uncertain behavior of bladder
D41.8 Neoplasm of uncertain behavior of other specified urinary organs
D41.9 Neoplasm of uncertain behavior of unspecified urinary organ
D42.0 Neoplasm of uncertain behavior of cerebral meninges
D42.1 Neoplasm of uncertain behavior of spinal meninges
D42.9 Neoplasm of uncertain behavior of meninges, unspecified
D43.0 Neoplasm of uncertain behavior of brain, 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 of brain, 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 of brain, unspecified
D43.3 Neoplasm of uncertain behavior of cranial nerves
D43.4 Neoplasm of uncertain behavior of spinal cord
D43.8 Neoplasm of uncertain behavior of other specified parts of central nervous system
D43.9 Neoplasm of uncertain behavior of central nervous system, unspecified
Includes: Neoplasm of uncertain behavior of nervous system (central) NOS
D44.0 Neoplasm of uncertain behavior of thyroid gland
D44.10 Neoplasm of uncertain behavior of unspecified adrenal gland
D44.11 Neoplasm of uncertain behavior of right adrenal gland
D44.12 Neoplasm of uncertain behavior of left adrenal gland
D44.2 Neoplasm of uncertain behavior of parathyroid gland
D44.3 Neoplasm of uncertain behavior of pituitary gland
D44.4 Neoplasm of uncertain behavior of craniopharyngeal duct
D44.5 Neoplasm of uncertain behavior of pineal gland
D44.6 Neoplasm of uncertain behavior of carotid body
D44.7 Neoplasm of uncertain behavior of aortic body and other paraganglia
D44.9 Neoplasm of uncertain behavior of unspecified 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 Primary thrombocytosis
Excludes 2: reactive thrombocytosis (D75.838) secondary thrombocytosis (D75.838) thrombocythemia NOS (D75.839) thrombocytosis NOS (D75.839)
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 of lymphoid, hematopoietic and related tissue, unspecified
Includes: Lymphoproliferative disease NOS
D48.0 Neoplasm of uncertain behavior of bone 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 of connective 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 of peripheral nerves and autonomic nervous system
Excludes 1: neoplasm of uncertain behavior of peripheral nerves of orbit (D48.7)
D48.3 Neoplasm of uncertain behavior of retroperitoneum
D48.4 Neoplasm of uncertain behavior of peritoneum
D48.5 Neoplasm of uncertain behavior of skin
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 of unspecified breast
D48.61 Neoplasm of uncertain behavior of right breast
D48.62 Neoplasm of uncertain behavior of left breast
D48.7 Neoplasm of uncertain behavior of other 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 due to intrinsic factor deficiency
Includes: Addison anemia Biermer anemia Pernicious (congenital) anemia Congenital intrinsic factor deficiency
D51.1 Vitamin B12 deficiency anemia due to 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-phosphate dehydrogenase [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 (vaso-occlusive) 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 (vaso-occlusive) 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 (vaso-occlusive) pain NOS
D57.42 Sickle-cell thalassemia beta zero without crisis
Includes: HbS-beta zero without crisis Sickle-cell beta zero without crisis
D57.431 Sickle-cell thalassemia beta zero with 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 zero with splenic sequestration
Includes: HbS-beta zero with splenic sequestration Sickle-cell beta zero with splenic sequestration
D57.433 Sickle-cell thalassemia beta zero with 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 zero with 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 zero with 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 (vaso-occlusive) pain NOS
D57.44 Sickle-cell thalassemia beta plus without crisis
Includes: HbS-beta plus without crisis Sickle-cell beta plus without crisis
D57.451 Sickle-cell thalassemia beta plus with 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 plus with splenic sequestration
Includes: HbS-beta plus with splenic sequestration Sickle-cell beta plus with splenic sequestration
D57.453 Sickle-cell thalassemia beta plus with 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 plus with 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 plus with 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 (vaso-occlusive) pain NOS
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 (vaso-occlusive) 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 hemolytic anemia
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: 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 due to disease
D64.2 Secondary sideroblastic anemia due to 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 2: anemia in neoplastic disease (D63.0) aplastic anemia due to antineoplastic chemotherapy (D61.1)
D64.89 Other specified anemias
Includes: Infantile pseudoleukemia
D64.9 Anemia, unspecified
D65 Disseminated intravascular coagulation [defibrination syndrome]
Includes: Afibrinogenemia, acquired Consumption coagulopathy COVID-19 associated diffuse or disseminated intravascular 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 to intrinsic 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: COVID-19 associated hypercoagulability Hypercoagulable states NEC Secondary hypercoagulable state NOS
D68.8 Other specified coagulation defects
Includes: COVID-19 associated coagulopathy
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: hemolytic-uremic syndrome (D59.3-)
Excludes 2: von Willebrand 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 white blood 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 blood and blood-forming organs
D75.9 Disease of blood and blood-forming organs, 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 Hemophagocytic syndrome, infection-associated
D76.3 Other histiocytosis syndromes
Includes: Reticulohistiocytoma (giant-cell) Sinus histiocytosis with massive lymphadenopathy Xanthogranuloma
D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere
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 laceration of the spleen during a procedure on the spleen
D78.12 Accidental puncture and laceration of 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 complications of the spleen
D78.89 Other postprocedural complications of 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 of infancy
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 carboxylase deficiency
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-limbed stature
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 conditions classified 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 in sarcoidosis
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-host disease
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 without goiter
Includes: Aplasia of thyroid (with myxedema) Congenital atrophy of thyroid Congenital hypothyroidism NOS
E03.2 Hypothyroidism due to medicaments and 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 goiter without thyrotoxic crisis or storm
E05.01 Thyrotoxicosis with diffuse goiter with 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
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