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75106 results found
| Q72.01 | Congenital complete absence of right lower limb |
| Q72.02 | Congenital complete absence of left lower limb |
| Q72.03 | Congenital complete absence of lower limb, bilateral |
| Q72.10 | Congenital absence of unspecified thigh and lower leg with foot present |
| Q72.11 | Congenital absence of right thigh and lower leg with foot present |
| Q72.12 | Congenital absence of left thigh and lower leg with foot present |
| Q72.13 | Congenital absence of thigh and lower leg with foot present, bilateral |
| Q72.20 | Congenital absence of both lower leg and foot, unspecified lower limb |
| Q72.21 | Congenital absence of both lower leg and foot, right lower limb |
| Q72.22 | Congenital absence of both lower leg and foot, left lower limb |
| Q72.23 | Congenital absence of both lower leg and foot, bilateral |
| Q72.30 | Congenital absence of unspecified foot and toe(s) |
| Q72.31 | Congenital absence of right foot and toe(s) |
| Q72.32 | Congenital absence of left foot and toe(s) |
| Q72.33 | Congenital absence of foot and toe(s), bilateral |
| Q72.40 | Longitudinal reduction defect of unspecified femur |
| Q72.41 | Longitudinal reduction defect of right femur |
| Q72.42 | Longitudinal reduction defect of left femur |
| Q72.43 | Longitudinal reduction defect of femur, bilateral |
| Q72.50 | Longitudinal reduction defect of unspecified tibia |
| Q72.51 | Longitudinal reduction defect of right tibia |
| Q72.52 | Longitudinal reduction defect of left tibia |
| Q72.53 | Longitudinal reduction defect of tibia, bilateral |
| Q72.60 | Longitudinal reduction defect of unspecified fibula |
| Q72.61 | Longitudinal reduction defect of right fibula |
| Q72.62 | Longitudinal reduction defect of left fibula |
| Q72.63 | Longitudinal reduction defect of fibula, bilateral |
| Q72.70 | Split foot, unspecified lower limb |
| Q72.71 | Split foot, right lower limb |
| Q72.72 | Split foot, left lower limb |
| Q72.73 | Split foot, bilateral |
| Q72.811 | Congenital shortening of right lower limb |
| Q72.812 | Congenital shortening of left lower limb |
| Q72.813 | Congenital shortening of lower limb, bilateral |
| Q72.819 | Congenital shortening of unspecified lower limb |
| Q72.891 | Other reduction defects of right lower limb |
| Q72.892 | Other reduction defects of left lower limb |
| Q72.893 | Other reduction defects of lower limb, bilateral |
| Q72.899 | Other reduction defects of unspecified lower limb |
| Q72.90 | Unspecified reduction defect of unspecified lower limb |
| Q72.91 | Unspecified reduction defect of right lower limb |
| Q72.92 | Unspecified reduction defect of left lower limb |
| Q72.93 | Unspecified reduction defect of lower limb, bilateral |
| Q73.0 |
Congenital absence of unspecified limb(s)
Includes: Amelia NOS |
| Q73.1 |
Phocomelia, unspecified limb(s)
Includes: Phocomelia NOS |
| Q73.8 |
Other reduction defects of unspecified limb(s)
Includes: Longitudinal reduction deformity of unspecified limb(s) Ectromelia of limb NOS Hemimelia of limb NOS Reduction defect of limb NOS |
| Q74.0 |
Other congenital malformations of upper limb(s), including shoulder girdle
Includes: Accessory carpal bones Cleidocranial dysostosis Congenital pseudarthrosis of clavicle Macrodactylia (fingers) Madelung's deformity Radioulnar synostosis Sprengel's deformity Triphalangeal thumb |
| Q74.1 |
Congenital malformation of knee
Includes: Congenital absence of patella Congenital dislocation of patella Congenital genu valgum Congenital genu varum Rudimentary patella Excludes 1: congenital dislocation of knee (Q68.2) congenital genu recurvatum (Q68.2) nail patella syndrome (Q87.2) |
| Q74.2 |
Other congenital malformations of lower limb(s), including pelvic girdle
Includes: Congenital fusion of sacroiliac joint Congenital malformation of ankle joint Congenital malformation of sacroiliac joint Excludes 1: anteversion of femur (neck) (Q65.89) |
| Q74.3 | Arthrogryposis multiplex congenita |
| Q74.8 | Other specified congenital malformations of limb(s) |
| Q74.9 |
Unspecified congenital malformation of limb(s)
Includes: Congenital anomaly of limb(s) NOS |
| Q75.0 |
Craniosynostosis
Includes: Acrocephaly Imperfect fusion of skull Oxycephaly Trigonocephaly |
| Q75.1 |
Craniofacial dysostosis
Includes: Crouzon's disease |
| Q75.2 | Hypertelorism |
| Q75.3 | Macrocephaly |
| Q75.4 |
Mandibulofacial dysostosis
Includes: Franceschetti syndrome Treacher Collins syndrome |
| Q75.5 | Oculomandibular dysostosis |
| Q75.8 |
Other specified congenital malformations of skull and face bones
Includes: Absence of skull bone, congenital Congenital deformity of forehead Platybasia |
| Q75.9 |
Congenital malformation of skull and face bones, unspecified
Includes: Congenital anomaly of face bones NOS Congenital anomaly of skull NOS |
| Q76.0 |
Spina bifida occulta
Excludes 1: meningocele (spinal) (Q05.-) spina bifida (aperta) (cystica) (Q05.-) |
| Q76.1 |
Klippel-Feil syndrome
Includes: Cervical fusion syndrome |
| Q76.2 |
Congenital spondylolisthesis
Includes: Congenital spondylolysis Excludes 1: spondylolisthesis (acquired) (M43.1-) spondylolysis (acquired) (M43.0-) |
| Q76.3 |
Congenital scoliosis due to congenital bony malformation
Includes: Hemivertebra fusion or failure of segmentation with scoliosis |
| Q76.411 | Congenital kyphosis, occipito-atlanto-axial region |
| Q76.412 | Congenital kyphosis, cervical region |
| Q76.413 | Congenital kyphosis, cervicothoracic region |
| Q76.414 | Congenital kyphosis, thoracic region |
| Q76.415 | Congenital kyphosis, thoracolumbar region |
| Q76.419 | Congenital kyphosis, unspecified region |
| Q76.425 | Congenital lordosis, thoracolumbar region |
| Q76.426 | Congenital lordosis, lumbar region |
| Q76.427 | Congenital lordosis, lumbosacral region |
| Q76.428 | Congenital lordosis, sacral and sacrococcygeal region |
| Q76.429 | Congenital lordosis, unspecified region |
| Q76.49 |
Other congenital malformations of spine, not associated with scoliosis
Includes: Congenital absence of vertebra NOS Congenital fusion of spine NOS Congenital malformation of lumbosacral (joint) (region) NOS Congenital malformation of spine NOS Hemivertebra NOS Malformation of spine NOS Platyspondylisis NOS Supernumerary vertebra NOS |
| Q76.5 |
Cervical rib
Includes: Supernumerary rib in cervical region |
| Q76.6 |
Other congenital malformations of ribs
Includes: Accessory rib Congenital absence of rib Congenital fusion of ribs Congenital malformation of ribs NOS Excludes 1: short rib syndrome (Q77.2) |
| Q76.7 |
Congenital malformation of sternum
Includes: Congenital absence of sternum Sternum bifidum |
| Q76.8 | Other congenital malformations of bony thorax |
| Q76.9 | Congenital malformation of bony thorax, unspecified |
| Q77.0 |
Achondrogenesis
Includes: Hypochondrogenesis |
| Q77.1 | Thanatophoric short stature |
| Q77.2 |
Short rib syndrome
Includes: Asphyxiating thoracic dysplasia [Jeune] |
| Q77.3 |
Chondrodysplasia punctata
Excludes 1: Rhizomelic chondrodysplasia punctata (E71.43) |
| Q77.4 |
Achondroplasia
Includes: Hypochondroplasia Osteosclerosis congenita |
| Q77.5 | Diastrophic dysplasia |
| Q77.6 |
Chondroectodermal dysplasia
Includes: Ellis-van Creveld syndrome |
| Q77.7 | Spondyloepiphyseal dysplasia |
| Q77.8 | Other osteochondrodysplasia with defects of growth of tubular bones and spine |
| Q77.9 | Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified |
| Q78.0 |
Osteogenesis imperfecta
Includes: Fragilitas ossium Osteopsathyrosis |
| Q78.1 |
Polyostotic fibrous dysplasia
Includes: Albright(-McCune)(-Sternberg) syndrome |
| Q78.2 |
Osteopetrosis
Includes: Albers-Schönberg syndrome Osteosclerosis NOS |
| Q78.3 |
Progressive diaphyseal dysplasia
Includes: Camurati-Engelmann syndrome |
| Q78.4 |
Enchondromatosis
Includes: Maffucci's syndrome Ollier's disease |
| Q78.5 |
Metaphyseal dysplasia
Includes: Pyle's syndrome |
| Q78.6 |
Multiple congenital exostoses
Includes: Diaphyseal aclasis |
| Q78.8 |
Other specified osteochondrodysplasias
Includes: Osteopoikilosis |
| Q78.9 |
Osteochondrodysplasia, unspecified
Includes: Chondrodystrophy NOS Osteodystrophy NOS |
| Q79.0 |
Congenital diaphragmatic hernia
Excludes 1: congenital hiatus hernia (Q40.1) |
| Q79.1 |
Other congenital malformations of diaphragm
Includes: Absence of diaphragm Congenital malformation of diaphragm NOS Eventration of diaphragm |
| Q79.2 |
Exomphalos
Includes: Omphalocele Excludes 1: umbilical hernia (K42.-) |
| Q79.3 | Gastroschisis |
| Q79.4 |
Prune belly syndrome
Includes: Congenital prolapse of bladder mucosa Eagle-Barrett syndrome |
| Q79.51 | Congenital hernia of bladder |
| Q79.59 | Other congenital malformations of abdominal wall |
| Q79.60 | Ehlers-Danlos syndrome, unspecified |
| Q79.61 |
Classical Ehlers-Danlos syndrome
Includes: Classical EDS (cEDS) |
| Q79.62 |
Hypermobile Ehlers-Danlos syndrome
Includes: Hypermobile EDS (hEDS) |
| Q79.63 |
Vascular Ehlers-Danlos syndrome
Includes: Vascular EDS (vEDS) |
| Q79.69 | Other Ehlers-Danlos syndromes |
| Q79.8 |
Other congenital malformations of musculoskeletal system
Includes: Absence of muscle Absence of tendon Accessory muscle Amyotrophia congenita Congenital constricting bands Congenital shortening of tendon Poland syndrome |
| Q79.9 |
Congenital malformation of musculoskeletal system, unspecified
Includes: Congenital anomaly of musculoskeletal system NOS Congenital deformity of musculoskeletal system NOS |
| Q80.0 | Ichthyosis vulgaris |
| Q80.1 | X-linked ichthyosis |
| Q80.2 |
Lamellar ichthyosis
Includes: Collodion baby |
| Q80.3 | Congenital bullous ichthyosiform erythroderma |
| Q80.4 | Harlequin fetus |
| Q80.8 | Other congenital ichthyosis |
| Q80.9 | Congenital ichthyosis, unspecified |
| Q81.0 |
Epidermolysis bullosa simplex
Excludes 1: Cockayne's syndrome (Q87.19) |
| Q81.1 |
Epidermolysis bullosa letalis
Includes: Herlitz' syndrome |
| Q81.2 | Epidermolysis bullosa dystrophica |
| Q81.8 | Other epidermolysis bullosa |
| Q81.9 | Epidermolysis bullosa, unspecified |
| Q82.0 | Hereditary lymphedema |
| Q82.1 | Xeroderma pigmentosum |
| Q82.2 |
Congenital cutaneous mastocytosis
Includes: Congenital diffuse cutaneous mastocytosis Congenital maculopapular cutaneous mastocytosis Congenital urticaria pigmentosa Excludes 1: cutaneous mastocytosis NOS (D47.01) diffuse cutaneous mastocytosis (with onset after newborn period) (D47.01) malignant mastocytosis (C96.2-) systemic mastocytosis (D47.02) urticaria pigmentosa (non-congenital) (with onset after newborn period) (D47.01) |
| Q82.3 | Incontinentia pigmenti |
| Q82.4 |
Ectodermal dysplasia (anhidrotic)
Excludes 1: Ellis-van Creveld syndrome (Q77.6) |
| Q82.5 |
Congenital non-neoplastic nevus
Includes: Birthmark NOS Flammeus Nevus Portwine Nevus Sanguineous Nevus Strawberry Nevus Vascular Nevus NOS Verrucous Nevus Excludes 2: Café au lait spots (L81.3) lentigo (L81.4) nevus NOS (D22.-) araneus nevus (I78.1) melanocytic nevus (D22.-) pigmented nevus (D22.-) spider nevus (I78.1) stellar nevus (I78.1) |
| Q82.6 |
Congenital sacral dimple
Includes: Parasacral dimple Excludes 2: pilonidal cyst with abscess (L05.01) pilonidal cyst without abscess (L05.91) |
| Q82.8 |
Other specified congenital malformations of skin
Includes: Abnormal palmar creases Accessory skin tags Benign familial pemphigus [Hailey-Hailey] Congenital poikiloderma Cutis laxa (hyperelastica) Dermatoglyphic anomalies Inherited keratosis palmaris et plantaris Keratosis follicularis [Darier-White] Excludes 1: Ehlers-Danlos syndromes (Q79.6-) |
| Q82.9 | Congenital malformation of skin, unspecified |
| Q83.0 | Congenital absence of breast with absent nipple |
| Q83.1 |
Accessory breast
Includes: Supernumerary breast |
| Q83.2 | Absent nipple |
| Q83.3 |
Accessory nipple
Includes: Supernumerary nipple |
| Q83.8 | Other congenital malformations of breast |
| Q83.9 | Congenital malformation of breast, unspecified |
| Q84.0 |
Congenital alopecia
Includes: Congenital atrichosis |
| Q84.1 |
Congenital morphological disturbances of hair, not elsewhere classified
Includes: Beaded hair Monilethrix Pili annulati Excludes 1: Menkes' kinky hair syndrome (E83.09) |
| Q84.2 |
Other congenital malformations of hair
Includes: Congenital hypertrichosis Congenital malformation of hair NOS Persistent lanugo |
| Q84.3 |
Anonychia
Excludes 1: nail patella syndrome (Q87.2) |
| Q84.4 | Congenital leukonychia |
| Q84.5 |
Enlarged and hypertrophic nails
Includes: Congenital onychauxis Pachyonychia |
| Q84.6 |
Other congenital malformations of nails
Includes: Congenital clubnail Congenital koilonychia Congenital malformation of nail NOS |
| Q84.8 |
Other specified congenital malformations of integument
Includes: Aplasia cutis congenita |
| Q84.9 |
Congenital malformation of integument, unspecified
Includes: Congenital anomaly of integument NOS Congenital deformity of integument NOS |
| Q85.00 | Neurofibromatosis, unspecified |
| Q85.01 |
Neurofibromatosis, type 1
Includes: Von Recklinghausen disease |
| Q85.02 |
Neurofibromatosis, type 2
Includes: Acoustic neurofibromatosis |
| Q85.03 | Schwannomatosis |
| Q85.09 | Other neurofibromatosis |
| Q85.1 |
Tuberous sclerosis
Includes: Bourneville's disease Epiloia |
| Q85.8 |
Other phakomatoses, not elsewhere classified
Includes: Peutz-Jeghers Syndrome Sturge-Weber(-Dimitri) syndrome von Hippel-Lindau syndrome Excludes 1: Meckel-Gruber syndrome (Q61.9) |
| Q85.9 |
Phakomatosis, unspecified
Includes: Hamartosis NOS |
| Q86.0 | Fetal alcohol syndrome (dysmorphic) |
| Q86.1 |
Fetal hydantoin syndrome
Includes: Meadow's syndrome |
| Q86.2 | Dysmorphism due to warfarin |
| Q86.8 | Other congenital malformation syndromes due to known exogenous causes |
| Q87.0 |
Congenital malformation syndromes predominantly affecting facial appearance
Includes: Acrocephalopolysyndactyly Acrocephalosyndactyly [Apert] Cryptophthalmos syndrome Cyclopia Goldenhar syndrome Moebius syndrome Oro-facial-digital syndrome Robin syndrome Whistling face |
| Q87.11 | Prader-Willi syndrome |
| Q87.19 |
Other congenital malformation syndromes predominantly associated with short stature
Includes: Aarskog syndrome Cockayne syndrome De Lange syndrome Dubowitz syndrome Noonan syndrome Robinow-Silverman-Smith syndrome Russell-Silver syndrome Seckel syndrome |
| Q87.2 |
Congenital malformation syndromes predominantly involving limbs
Includes: Holt-Oram syndrome Klippel-Trenaunay-Weber syndrome Nail patella syndrome Rubinstein-Taybi syndrome Sirenomelia syndrome Thrombocytopenia with absent radius [TAR] syndrome VATER syndrome |
| Q87.3 |
Congenital malformation syndromes involving early overgrowth
Includes: Beckwith-Wiedemann syndrome Sotos syndrome Weaver syndrome |
| Q87.40 | Marfan syndrome, unspecified |
| Q87.410 | Marfan syndrome with aortic dilation |
| Q87.418 | Marfan syndrome with other cardiovascular manifestations |
| Q87.42 | Marfan syndrome with ocular manifestations |
| Q87.43 | Marfan syndrome with skeletal manifestation |
| Q87.5 | Other congenital malformation syndromes with other skeletal changes |
| Q87.81 | Alport syndrome |
| Q87.82 | Arterial tortuosity syndrome |
| Q87.89 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q89.01 | Asplenia (congenital) |
| Q89.09 |
Congenital malformations of spleen
Includes: Congenital splenomegaly |
| Q89.1 |
Congenital malformations of adrenal gland
Excludes 1: adrenogenital disorders (E25.-) congenital adrenal hyperplasia (E25.0) |
| Q89.2 |
Congenital malformations of other endocrine glands
Includes: Congenital malformation of parathyroid or thyroid gland Persistent thyroglossal duct Thyroglossal cyst Excludes 1: congenital goiter (E03.0) congenital hypothyroidism (E03.1) |
| Q89.3 |
Situs inversus
Includes: Dextrocardia with situs inversus Mirror-image atrial arrangement with situs inversus Situs inversus or transversus abdominalis Situs inversus or transversus thoracis Transposition of abdominal viscera Transposition of thoracic viscera Excludes 1: dextrocardia NOS (Q24.0) |
| Q89.4 |
Conjoined twins
Includes: Craniopagus Dicephaly Pygopagus Thoracopagus |
| Q89.7 |
Multiple congenital malformations, not elsewhere classified
Includes: Multiple congenital anomalies NOS Multiple congenital deformities NOS Excludes 1: congenital malformation syndromes affecting multiple systems (Q87.-) |
| Q89.8 | Other specified congenital malformations |
| Q89.9 |
Congenital malformation, unspecified
Includes: Congenital anomaly NOS Congenital deformity NOS |
| Q90.0 | Trisomy 21, nonmosaicism (meiotic nondisjunction) |
| Q90.1 | Trisomy 21, mosaicism (mitotic nondisjunction) |
| Q90.2 | Trisomy 21, translocation |
| Q90.9 |
Down syndrome, unspecified
Includes: Trisomy 21 NOS |
| Q91.0 | Trisomy 18, nonmosaicism (meiotic nondisjunction) |
| Q91.1 | Trisomy 18, mosaicism (mitotic nondisjunction) |
| Q91.2 | Trisomy 18, translocation |
| Q91.3 | Trisomy 18, unspecified |
| Q91.4 | Trisomy 13, nonmosaicism (meiotic nondisjunction) |
| Q91.5 | Trisomy 13, mosaicism (mitotic nondisjunction) |
| Q91.6 | Trisomy 13, translocation |
| Q91.7 | Trisomy 13, unspecified |
| Q92.0 | Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction) |
| Q92.1 | Whole chromosome trisomy, mosaicism (mitotic nondisjunction) |
| Q92.2 |
Partial trisomy
Includes: Less than whole arm duplicated Whole arm or more duplicated Excludes 1: partial trisomy due to unbalanced translocation (Q92.5) |
| Q92.5 |
Duplications with other complex rearrangements
Includes: Partial trisomy due to unbalanced translocations |
| Q92.61 | Marker chromosomes in normal individual |
| Q92.62 | Marker chromosomes in abnormal individual |
| Q92.7 | Triploidy and polyploidy |
| Q92.8 |
Other specified trisomies and partial trisomies of autosomes
Includes: Duplications identified by fluorescence in situ hybridization (FISH) Duplications identified by in situ hybridization (ISH) Duplications seen only at prometaphase |
| Q92.9 | Trisomy and partial trisomy of autosomes, unspecified |
| Q93.0 | Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction) |
| Q93.1 | Whole chromosome monosomy, mosaicism (mitotic nondisjunction) |
| Q93.2 | Chromosome replaced with ring, dicentric or isochromosome |
| Q93.3 |
Deletion of short arm of chromosome 4
Includes: Wolff-Hirschorn syndrome |
| Q93.4 |
Deletion of short arm of chromosome 5
Includes: Cri-du-chat syndrome |
| Q93.51 | Angelman syndrome |
| Q93.59 | Other deletions of part of a chromosome |
| Q93.7 |
Deletions with other complex rearrangements
Includes: Deletions due to unbalanced translocations, inversions and insertions |
| Q93.81 |
Velo-cardio-facial syndrome
Includes: Deletion 22q11.2 |
| Q93.82 | Williams syndrome |
| Q93.88 |
Other microdeletions
Includes: Miller-Dieker syndrome Smith-Magenis syndrome |
| Q93.89 |
Other deletions from the autosomes
Includes: Deletions identified by fluorescence in situ hybridization (FISH) Deletions identified by in situ hybridization (ISH) Deletions seen only at prometaphase |
| Q93.9 | Deletion from autosomes, unspecified |
| Q95.0 | Balanced translocation and insertion in normal individual |
| Q95.1 | Chromosome inversion in normal individual |
| Q95.2 | Balanced autosomal rearrangement in abnormal individual |
| Q95.3 | Balanced sex/autosomal rearrangement in abnormal individual |
| Q95.5 | Individual with autosomal fragile site |
| Q95.8 | Other balanced rearrangements and structural markers |
| Q95.9 | Balanced rearrangement and structural marker, unspecified |
| Q96.0 | Karyotype 45, X |
| Q96.1 |
Karyotype 46, X iso (Xq)
Includes: Karyotype 46, isochromosome Xq |
| Q96.2 |
Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
Includes: Karyotype 46, X with abnormal sex chromosome, except isochromosome Xq |
| Q96.3 | Mosaicism, 45, X/46, XX or XY |
| Q96.4 | Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome |
| Q96.8 | Other variants of Turner's syndrome |
| Q96.9 | Turner's syndrome, unspecified |
| Q97.0 | Karyotype 47, XXX |
| Q97.1 | Female with more than three X chromosomes |
| Q97.2 | Mosaicism, lines with various numbers of X chromosomes |
| Q97.3 | Female with 46, XY karyotype |
| Q97.8 | Other specified sex chromosome abnormalities, female phenotype |
| Q97.9 | Sex chromosome abnormality, female phenotype, unspecified |
| Q98.0 | Klinefelter syndrome karyotype 47, XXY |
| Q98.1 | Klinefelter syndrome, male with more than two X chromosomes |
| Q98.3 | Other male with 46, XX karyotype |
| Q98.4 | Klinefelter syndrome, unspecified |
| Q98.5 | Karyotype 47, XYY |
| Q98.6 | Male with structurally abnormal sex chromosome |
| Q98.7 | Male with sex chromosome mosaicism |
| Q98.8 | Other specified sex chromosome abnormalities, male phenotype |
| Q98.9 | Sex chromosome abnormality, male phenotype, unspecified |
| Q99.0 |
Chimera 46, XX/46, XY
Includes: Chimera 46, XX/46, XY true hermaphrodite |
| Q99.1 |
46, XX true hermaphrodite
Includes: 46, XX with streak gonads 46, XY with streak gonads Pure gonadal dysgenesis |
| Q99.2 |
Fragile X chromosome
Includes: Fragile X syndrome |
| Q99.8 | Other specified chromosome abnormalities |
| Q99.9 | Chromosomal abnormality, unspecified |
| R00.0 |
Tachycardia, unspecified
Includes: Rapid heart beat Sinoauricular tachycardia NOS Sinus [sinusal] tachycardia NOS Excludes 1: inappropriate sinus tachycardia, so stated (I47.11) neonatal tachycardia (P29.11) paroxysmal tachycardia (I47.-) |
| R00.1 |
Bradycardia, unspecified
Includes: Sinoatrial bradycardia Sinus bradycardia Slow heart beat Vagal bradycardia Excludes 1: neonatal bradycardia (P29.12) |
| R00.2 |
Palpitations
Includes: Awareness of heart beat |
| R00.8 | Other abnormalities of heart beat |
| R00.9 | Unspecified abnormalities of heart beat |
| R01.0 |
Benign and innocent cardiac murmurs
Includes: Functional cardiac murmur |
| R01.1 |
Cardiac murmur, unspecified
Includes: Cardiac bruit NOS Heart murmur NOS Systolic murmur NOS |
| R01.2 |
Other cardiac sounds
Includes: Cardiac dullness, increased or decreased Precordial friction |
| R03.0 | Elevated blood-pressure reading, without diagnosis of hypertension |
| R03.1 |
Nonspecific low blood-pressure reading
Excludes 1: hypotension (I95.-) maternal hypotension syndrome (O26.5-) neurogenic orthostatic hypotension (G90.3) |
| R04.0 |
Epistaxis
Includes: Hemorrhage from nose Nosebleed |
| R04.1 |
Hemorrhage from throat
Excludes 2: hemoptysis (R04.2) |
| R04.2 |
Hemoptysis
Includes: Blood-stained sputum Cough with hemorrhage |
| R04.81 |
Acute idiopathic pulmonary hemorrhage in infants
Includes: AIPHI Acute idiopathic hemorrhage in infants over 28 days old Excludes 1: perinatal pulmonary hemorrhage (P26.-) von Willebrand disease (D68.0-) |
| R04.89 |
Hemorrhage from other sites in respiratory passages
Includes: Pulmonary hemorrhage NOS |
| R04.9 | Hemorrhage from respiratory passages, unspecified |
| R05 |
Cough
Excludes 1: cough with hemorrhage (R04.2) smoker's cough (J41.0) |
| R06.00 | Dyspnea, unspecified |
| R06.01 | Orthopnea |
| R06.02 | Shortness of breath |
| R06.03 | Acute respiratory distress |
| R06.09 | Other forms of dyspnea |
| R06.1 |
Stridor
Excludes 1: congenital laryngeal stridor (P28.89) laryngismus (stridulus) (J38.5) |
| R06.2 |
Wheezing
Excludes 1: Asthma (J45.-) |
| R06.3 |
Periodic breathing
Includes: Cheyne-Stokes breathing |
| R06.4 |
Hyperventilation
Excludes 1: psychogenic hyperventilation (F45.8) |
| R06.5 |
Mouth breathing
Excludes 2: dry mouth NOS (R68.2) |
| R06.6 |
Hiccough
Excludes 1: psychogenic hiccough (F45.8) |
| R06.7 | Sneezing |
| R06.81 |
Apnea, not elsewhere classified
Includes: Apnea NOS Excludes 1: apnea (of) newborn (P28.4-) sleep apnea (G47.3-) sleep apnea of newborn (primary) (P28.3-) |
| R06.82 |
Tachypnea, not elsewhere classified
Includes: Tachypnea NOS Excludes 1: transitory tachypnea of newborn (P22.1) |
| R06.83 | Snoring |
| R06.89 |
Other abnormalities of breathing
Includes: Breath-holding (spells) Sighing |
| R06.9 | Unspecified abnormalities of breathing |
| R07.0 |
Pain in throat
Excludes 1: chronic sore throat (J31.2) sore throat (acute) NOS (J02.9) Excludes 2: dysphagia (R13.1-) pain in neck (M54.2) |
| R07.1 |
Chest pain on breathing
Includes: Painful respiration |
| R07.2 | Precordial pain |
| R07.81 |
Pleurodynia
Includes: Pleurodynia NOS Excludes 1: epidemic pleurodynia (B33.0) |
| R07.82 | Intercostal pain |
| R07.89 |
Other chest pain
Includes: Anterior chest-wall pain NOS |
| R07.9 | Chest pain, unspecified |
| R09.01 | Asphyxia |
| R09.02 | Hypoxemia |
| R09.1 |
Pleurisy
Excludes 1: pleurisy with effusion (J90) |
| R09.2 |
Respiratory arrest
Includes: Cardiorespiratory failure Excludes 1: cardiac arrest (I46.-) respiratory arrest of newborn (P28.81) respiratory distress of newborn (P22.0) respiratory failure (J96.-) respiratory failure of newborn (P28.5) respiratory insufficiency (R06.89) respiratory insufficiency of newborn (P28.5) |
| R09.3 |
Abnormal sputum
Includes: Abnormal amount of sputum Abnormal color of sputum Abnormal odor of sputum Excessive sputum Excludes 1: blood-stained sputum (R04.2) |
| R09.81 | Nasal congestion |
| R09.82 | Postnasal drip |
| R09.89 |
Other specified symptoms and signs involving the circulatory and respiratory systems
Includes: Abnormal chest percussion Bruit (arterial) Chest tympany Choking sensation Friction sounds in chest Rales Weak pulse Excludes 2: foreign body in throat (T17.2-) wheezing (R06.2) |
| R10.0 |
Acute abdomen
Includes: Severe abdominal pain (generalized) (with abdominal rigidity) Excludes 1: abdominal rigidity NOS (R19.3) generalized abdominal pain NOS (R10.84) localized abdominal pain (R10.1-R10.3-) |
| R10.10 | Upper abdominal pain, unspecified |
| R10.11 | Right upper quadrant pain |
| R10.12 | Left upper quadrant pain |
| R10.13 |
Epigastric pain
Includes: Dyspepsia Excludes 1: functional dyspepsia (K30) |
| R10.2 |
Pelvic and perineal pain
Excludes 1: vulvodynia (N94.81) |
| R10.30 | Lower abdominal pain, unspecified |
| R10.31 | Right lower quadrant pain |
| R10.32 | Left lower quadrant pain |
| R10.33 | Periumbilical pain |
| R10.811 | Right upper quadrant abdominal tenderness |
| R10.812 | Left upper quadrant abdominal tenderness |
| R10.813 | Right lower quadrant abdominal tenderness |
| R10.814 | Left lower quadrant abdominal tenderness |
| R10.815 | Periumbilic abdominal tenderness |
| R10.816 | Epigastric abdominal tenderness |
| R10.817 | Generalized abdominal tenderness |
| R10.819 | Abdominal tenderness, unspecified site |
| R10.821 | Right upper quadrant rebound abdominal tenderness |
| R10.822 | Left upper quadrant rebound abdominal tenderness |
| R10.823 | Right lower quadrant rebound abdominal tenderness |
| R10.824 | Left lower quadrant rebound abdominal tenderness |
| R10.825 | Periumbilic rebound abdominal tenderness |
| R10.826 | Epigastric rebound abdominal tenderness |
| R10.827 | Generalized rebound abdominal tenderness |
| R10.829 | Rebound abdominal tenderness, unspecified site |
| R10.83 |
Colic
Includes: Colic NOS Infantile colic Excludes 1: colic in adult and child over 12 months old (R10.84) |
| R10.84 |
Generalized abdominal pain
Excludes 1: generalized abdominal pain associated with acute abdomen (R10.0) |
| R10.9 | Unspecified abdominal pain |
| R11.0 |
Nausea
Includes: Nausea NOS Nausea without vomiting |
| R11.10 |
Vomiting, unspecified
Includes: Vomiting NOS |
| R11.11 | Vomiting without nausea |
| R11.12 | Projectile vomiting |
| R11.13 | Vomiting of fecal matter |
| R11.14 |
Bilious vomiting
Includes: Bilious emesis |
| R11.15 |
Cyclical vomiting syndrome unrelated to migraine
Includes: Cyclic vomiting syndrome NOS Persistent vomiting Excludes 1: cyclical vomiting in migraine (G43.A-) Excludes 2: bulimia nervosa (F50.20) diabetes mellitus due to underlying condition (E08.-) |
| R11.2 |
Nausea with vomiting, unspecified
Includes: Persistent nausea with vomiting NOS |
| R12 |
Heartburn
Excludes 1: dyspepsia NOS (R10.13) functional dyspepsia (K30) |
| R13.0 |
Aphagia
Includes: Inability to swallow Excludes 1: psychogenic aphagia (F50.9) |
| R13.10 |
Dysphagia, unspecified
Includes: Difficulty in swallowing NOS |
| R13.11 | Dysphagia, oral phase |
| R13.12 | Dysphagia, oropharyngeal phase |
| R13.13 | Dysphagia, pharyngeal phase |
| R13.14 | Dysphagia, pharyngoesophageal phase |
| R13.19 |
Other dysphagia
Includes: Cervical dysphagia Neurogenic dysphagia |
| R14.0 |
Abdominal distension (gaseous)
Includes: Bloating Tympanites (abdominal) (intestinal) |
| R14.1 | Gas pain |
| R14.2 | Eructation |
| R14.3 | Flatulence |
| R15.0 |
Incomplete defecation
Excludes 1: constipation (K59.0-) fecal impaction (K56.41) |
| R15.1 |
Fecal smearing
Includes: Fecal soiling |
| R15.2 | Fecal urgency |
| R15.9 |
Full incontinence of feces
Includes: Fecal incontinence NOS |
| R16.0 |
Hepatomegaly, not elsewhere classified
Includes: Hepatomegaly NOS |
| R16.1 |
Splenomegaly, not elsewhere classified
Includes: Splenomegaly NOS |
| R16.2 |
Hepatomegaly with splenomegaly, not elsewhere classified
Includes: Hepatosplenomegaly NOS |
| R17 |
Unspecified jaundice
Excludes 1: neonatal jaundice (P55, P57-P59) |
| R18.0 | Malignant ascites |
| R18.8 |
Other ascites
Includes: Ascites NOS Peritoneal effusion (chronic) |
| R19.00 | Intra-abdominal and pelvic swelling, mass and lump, unspecified site |
| R19.01 | Right upper quadrant abdominal swelling, mass and lump |
| R19.02 | Left upper quadrant abdominal swelling, mass and lump |
| R19.03 | Right lower quadrant abdominal swelling, mass and lump |
| R19.04 | Left lower quadrant abdominal swelling, mass and lump |
| R19.05 |
Periumbilic swelling, mass or lump
Includes: Diffuse or generalized umbilical swelling or mass |
| R19.06 | Epigastric swelling, mass or lump |
| R19.07 |
Generalized intra-abdominal and pelvic swelling, mass and lump
Includes: Diffuse or generalized intra-abdominal swelling or mass NOS Diffuse or generalized pelvic swelling or mass NOS |
| R19.09 | Other intra-abdominal and pelvic swelling, mass and lump |
| R19.11 | Absent bowel sounds |
| R19.12 | Hyperactive bowel sounds |
| R19.15 |
Other abnormal bowel sounds
Includes: Abnormal bowel sounds NOS |
| R19.2 |
Visible peristalsis
Includes: Hyperperistalsis |
| R19.30 | Abdominal rigidity, unspecified site |
| R19.31 | Right upper quadrant abdominal rigidity |
| R19.32 | Left upper quadrant abdominal rigidity |
| R19.33 | Right lower quadrant abdominal rigidity |
| R19.34 | Left lower quadrant abdominal rigidity |
| R19.35 | Periumbilic abdominal rigidity |
| R19.36 | Epigastric abdominal rigidity |
| R19.37 | Generalized abdominal rigidity |
| R19.4 |
Change in bowel habit
Excludes 1: constipation (K59.0-) functional diarrhea (K59.1) |
| R19.5 |
Other fecal abnormalities
Includes: Abnormal stool color Bulky stools Mucus in stools Occult blood in feces Occult blood in stools Excludes 1: melena (K92.1) neonatal melena (P54.1) |
| R19.6 | Halitosis |
| R19.7 |
Diarrhea, unspecified
Includes: Diarrhea NOS Excludes 1: functional diarrhea (K59.1) neonatal diarrhea (P78.3) psychogenic diarrhea (F45.8) |
| R19.8 | Other specified symptoms and signs involving the digestive system and abdomen |
| R20.0 | Anesthesia of skin |
| R20.1 | Hypoesthesia of skin |
| R20.2 |
Paresthesia of skin
Includes: Formication Pins and needles Tingling skin Excludes 1: acroparesthesia (I73.8) |
| R20.3 | Hyperesthesia |
| R20.8 | Other disturbances of skin sensation |
| R20.9 | Unspecified disturbances of skin sensation |
| R21 |
Rash and other nonspecific skin eruption
Excludes 1: specified type of rash- code to condition vesicular eruption (R23.8) |
| R22.0 | Localized swelling, mass and lump, head |
| R22.1 | Localized swelling, mass and lump, neck |
| R22.2 |
Localized swelling, mass and lump, trunk
Excludes 1: intra-abdominal or pelvic mass and lump (R19.0-) intra-abdominal or pelvic swelling (R19.0-) Excludes 2: breast mass and lump (N63) |
| R22.30 | Localized swelling, mass and lump, unspecified upper limb |
| R22.31 | Localized swelling, mass and lump, right upper limb |
| R22.32 | Localized swelling, mass and lump, left upper limb |
| R22.33 | Localized swelling, mass and lump, upper limb, bilateral |
| R22.40 | Localized swelling, mass and lump, unspecified lower limb |
| R22.41 | Localized swelling, mass and lump, right lower limb |
| R22.42 | Localized swelling, mass and lump, left lower limb |
| R22.43 | Localized swelling, mass and lump, lower limb, bilateral |
| R22.9 | Localized swelling, mass and lump, unspecified |
| R23.0 |
Cyanosis
Excludes 1: acrocyanosis (I73.8) cyanotic attacks of newborn (P28.2) |
| R23.1 |
Pallor
Includes: Clammy skin |
| R23.2 |
Flushing
Includes: Excessive blushing |
| R23.3 |
Spontaneous ecchymoses
Includes: Petechiae Excludes 1: ecchymoses of newborn (P54.5) purpura (D69.-) |
| R23.4 |
Changes in skin texture
Includes: Desquamation of skin Induration of skin Scaling of skin Excludes 1: epidermal thickening NOS (L85.9) |
| R23.8 | Other skin changes |
| R23.9 | Unspecified skin changes |
| R25.0 | Abnormal head movements |
| R25.1 |
Tremor, unspecified
Excludes 1: chorea NOS (G25.5) essential tremor (G25.0) hysterical tremor (F44.4) intention tremor (G25.2) |
| R25.2 |
Cramp and spasm
Excludes 2: carpopedal spasm (R29.0) charley-horse (M62.831) infantile spasms (G40.4-) muscle spasm of back (M62.830) muscle spasm of calf (M62.831) |
| R25.3 |
Fasciculation
Includes: Twitching NOS |
| R25.8 | Other abnormal involuntary movements |
| R25.9 | Unspecified abnormal involuntary movements |
| R26.0 |
Ataxic gait
Includes: Staggering gait |
| R26.1 |
Paralytic gait
Includes: Spastic gait |
| R26.2 |
Difficulty in walking, not elsewhere classified
Excludes 1: falling (R29.6) unsteadiness on feet (R26.81) |
| R26.81 | Unsteadiness on feet |
| R26.89 | Other abnormalities of gait and mobility |
| R26.9 | Unspecified abnormalities of gait and mobility |
| R27.0 |
Ataxia, unspecified
Excludes 1: ataxia following cerebrovascular disease (I69. with final characters -93) |
| R27.8 | Other lack of coordination |
| R27.9 | Unspecified lack of coordination |
| R29.0 |
Tetany
Includes: Carpopedal spasm Excludes 1: hysterical tetany (F44.5) neonatal tetany (P71.3) parathyroid tetany (E20.9) post-thyroidectomy tetany (E89.2) |
| R29.1 | Meningismus |
| R29.2 |
Abnormal reflex
Excludes 2: abnormal pupillary reflex (H57.0) hyperactive gag reflex (J39.2) vasovagal reaction or syncope (R55) |
| R29.3 | Abnormal posture |
| R29.4 |
Clicking hip
Excludes 1: congenital deformities of hip (Q65.-) |
| R29.5 |
Transient paralysis
Excludes 1: transient ischemic attack (G45.9) |
| R29.6 |
Repeated falls
Includes: Falling Tendency to fall Excludes 2: at risk for falling (Z91.81) history of falling (Z91.81) |
| R29.700 | NIHSS score 0 |
| R29.701 | NIHSS score 1 |
| R29.702 | NIHSS score 2 |
| R29.703 | NIHSS score 3 |
| R29.704 | NIHSS score 4 |
| R29.705 | NIHSS score 5 |
| R29.706 | NIHSS score 6 |
| R29.707 | NIHSS score 7 |
| R29.708 | NIHSS score 8 |
| R29.709 | NIHSS score 9 |
| R29.710 | NIHSS score 10 |
| R29.711 | NIHSS score 11 |
| R29.712 | NIHSS score 12 |
| R29.713 | NIHSS score 13 |
| R29.714 | NIHSS score 14 |
| R29.715 | NIHSS score 15 |
| R29.716 | NIHSS score 16 |
| R29.717 | NIHSS score 17 |
| R29.718 | NIHSS score 18 |
| R29.719 | NIHSS score 19 |
| R29.720 | NIHSS score 20 |
| R29.721 | NIHSS score 21 |
| R29.722 | NIHSS score 22 |
| R29.723 | NIHSS score 23 |
| R29.724 | NIHSS score 24 |
| R29.725 | NIHSS score 25 |
| R29.726 | NIHSS score 26 |
| R29.727 | NIHSS score 27 |
| R29.728 | NIHSS score 28 |
| R29.729 | NIHSS score 29 |
| R29.730 | NIHSS score 30 |
| R29.731 | NIHSS score 31 |
| R29.732 | NIHSS score 32 |
| R29.733 | NIHSS score 33 |
| R29.734 | NIHSS score 34 |
| R29.735 | NIHSS score 35 |
| R29.736 | NIHSS score 36 |
| R29.737 | NIHSS score 37 |
| R29.738 | NIHSS score 38 |
| R29.739 | NIHSS score 39 |
| R29.740 | NIHSS score 40 |
| R29.741 | NIHSS score 41 |
| R29.742 | NIHSS score 42 |
| R29.810 |
Facial weakness
Includes: Facial droop Excludes 1: Bell's palsy (G51.0) facial weakness following cerebrovascular disease (I69. with final characters -92) |
| R29.818 | Other symptoms and signs involving the nervous system |
| R29.890 |
Loss of height
Excludes 1: osteoporosis (M80-M81) |
| R29.891 |
Ocular torticollis
Excludes 1: congenital (sternomastoid) torticollis Q68.0 psychogenic torticollis (F45.8) spasmodic torticollis (G24.3) torticollis due to birth injury (P15.8) torticollis NOS M43.6 |
| R29.898 | Other symptoms and signs involving the musculoskeletal system |
| R29.90 | Unspecified symptoms and signs involving the nervous system |
| R29.91 | Unspecified symptoms and signs involving the musculoskeletal system |
| R30.0 |
Dysuria
Includes: Strangury |
| R30.1 | Vesical tenesmus |
| R30.9 |
Painful micturition, unspecified
Includes: Painful urination NOS |
| R31.0 | Gross hematuria |
| R31.1 | Benign essential microscopic hematuria |
| R31.21 |
Asymptomatic microscopic hematuria
Includes: AMH |
| R31.29 | Other microscopic hematuria |
| R31.9 | Hematuria, unspecified |
| R32 |
Unspecified urinary incontinence
Includes: Enuresis NOS Excludes 1: functional urinary incontinence (R39.81) nonorganic enuresis (F98.0) stress incontinence and other specified urinary incontinence (N39.3-N39.4-) urinary incontinence associated with cognitive impairment (R39.81) |
| R33.0 | Drug induced retention of urine |
| R33.8 | Other retention of urine |
| R33.9 | Retention of urine, unspecified |
| R34 |
Anuria and oliguria
Excludes 1: anuria and oliguria complicating abortion or ectopic or molar pregnancy (O00-O07, O08.4) anuria and oliguria complicating pregnancy (O26.83-) anuria and oliguria complicating the puerperium (O90.49) |
| R35.0 | Frequency of micturition |
| R35.1 | Nocturia |