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List of ICD-9 codes 740-759: Congenital anomalies
14. Congenital anomalies (740-759)
nervous system
eye, ear, face and neck
circulatory system
- (745) Bulbus cordis anomalies and anomalies of cardiac septal closure
- (747) Other congenital anomalies of circulatory system
- (747.1) Coarctation of aorta
- (747.2) Other congenital anomalies of aorta
- (747.3) Congenital anomalies of pulmonary artery
- (747.4) Congenital anomalies of great veins
- (747.5) Absence or hypoplasia of umbilical artery
- (747.6) Arteriovenous malformation, unspec.
- (747.8) Other specified anomalies of circulatory system
- (747.81) Arteriovenous malformation of brain
- (746.82) Cor triatriatum
- (746.83) Infundibular pulmonic stenosis congenital
- (746.84) Congenital obstructive anomalies of heart not elsewhere classified
- (746.85) Coronary artery anomaly congenital
- (746.86) Congenital heart block
- (746.87) Malposition of heart and cardiac apex
- (747.89) Other specified congenital anomalies of heart
- (747.9) Unspecified congenital anomaly of circulatory system
respiratory system
digestive system
- (749) Cleft palate
- (749.0) Cleft palate, unspec.
- (749.2) Cleft palate w/ cleft lip
genital organs
urinary system
musculoskeletal system
- (754) Certain congenital musculoskeletal deformities
- (755) Other congenital anomalies of limbs
- (755.0) Polydactyly
- (755.5) Other congenital anomalies of upper limb including shoulder girdle
- (755.9) Limb anomaly, unspec.
- (756) Other congenital musculoskeletal anomalies
- (756.1) Anomalies of spine
- (756.5) Osteodystrophies
integument
chromosomal anomalies
Other
See also
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Congenital malformations and deformations of circulatory system (Q20-Q28, 745-747) |
| Cardiac chambers and connections |
Persistent truncus arteriosus - Double outlet right ventricle (Taussig-Bing syndrome) - Transposition of the great vessels (dextro, levo) |
| Cardiac septa |
Ventricular septal defect - Atrial septal defect (Lutembacher's syndrome) - Atrioventricular septal defect (Ostium primum) - Tetralogy of Fallot - Eisenmenger's syndrome |
| Right: pulmonary and tricuspid valves |
pulmonary valves (stenosis, insufficiency) - tricuspid valves (stenosis, atresia) - Ebstein's anomaly |
| Left: aortic and mitral valves |
aortic valves (stenosis, insufficiency, bicuspid) - mitral valves (stenosis, regurgitation) - Hypoplastic left heart syndrome |
Other congenital malformations
of heart |
Dextrocardia - Levocardia - Cor triatriatum |
| Great arteries |
aorta (Patent ductus arteriosus, Aortic coarctation, Interrupted aortic arch, Overriding aorta, Aneurysm of sinus of Valsalva, Vascular ring) - Pulmonary atresia |
| Great veins |
Persistent left superior vena cava - Total anomalous pulmonary venous connection - Scimitar syndrome |
| Other |
Arteriovenous malformation (Cerebral arteriovenous malformation) |
| See also non-congenital conditions (I, 390-459) |
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Congenital malformations and deformations of musculoskeletal system (Q65-Q79, 754-756) |
| Limbs |
hip: Dislocation of hip/Hip dysplasia
feet (Club foot, Flat feet, Pes cavus)
head, face, spine and chest: skull, face and jaw (Dolichocephaly, Plagiocephaly) - Scoliosis - chest (Pectus excavatum, Pectus carinatum)
Polydactyly/Syndactyly (Webbed toes)
reduction deficits (Ectrodactyly, Amelia, Phocomelia)
upper limb (Cleidocranial dysostosis, Madelung's deformity, Sprengel's deformity)
knee (Genu valgum, Genu varum)
Arthrogryposis |
| Skull and face bones |
Craniosynostosis (Scaphocephaly) - Trigonocephaly - Oxycephaly - Crouzon syndrome - Hypertelorism - Macrocephaly - Treacher Collins syndrome - Platybasia |
| Spine and bony thorax |
Klippel-Feil syndrome - Spondylolisthesis - Cervical rib - Bifid rib |
| Osteochondrodysplasia |
growth of tubular bones and spine: Achondrogenesis - Thanatophoric dysplasia - Short rib-polydactyly syndrome - Chondrodysplasia punctata (Rhizomelic chondrodysplasia punctata, Conradi-Hünermann syndrome), Achondroplasia (Hypochondroplasia, Osteosclerosis congenita) - Ellis-van Creveld syndrome - Spondyloepiphyseal dysplasia congenita
Osteogenesis imperfecta - McCune-Albright syndrome - Osteopetrosis - Metaphyseal dysplasia - Hereditary multiple exostoses - Osteopoikilosis - Chondrodystrophy - Osteodystrophy |
| Other |
abdominal wall (Congenital diaphragmatic hernia, Omphalocele, Gastroschisis, Prune belly syndrome) - Ehlers-Danlos syndrome |
| See also non-congenital conditions (M, 710-739) |
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Pathology: chromosome abnormalities (Q90-Q99, 758) |
| Autosomal trisomies |
Down syndrome (21), Edwards syndrome (18), Patau syndrome (13), Trisomy 9, Warkany syndrome 2 (8), Cat eye syndrome (22) |
| Autosomal monosomies/deletions |
Wolf-Hirschhorn syndrome (4), Cri du chat (5), Angelman syndrome/Prader-Willi syndrome (15), Miller-Dieker syndrome/Smith-Magenis syndrome (17), 22q11.2 deletion syndrome (22) |
| X/Y linked |
Monosomy: Turner syndrome (XO)
Trisomy: Triple X syndrome (XXX), Klinefelter's syndrome (XXY), XYY |
| Translocations |
Philadelphia chromosome, Burkitt's lymphoma |
| Other |
Fragile X syndrome, Gonadal dysgenesis (Mixed gonadal dysgenesis) |
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Phakomatoses and other congenital malformations not elsewhere classified (Q85-Q89, 759) |
| Phakomatoses |
Neurofibromatosis (type I, type II) - Tuberous sclerosis - Peutz-Jeghers syndrome - Sturge-Weber syndrome - Von Hippel-Lindau disease - Incontinentia pigmenti - Ataxia telangiectasia |
| Due to known exogenous causes |
Fetal alcohol syndrome - Phocomelia (via Thalidomide) |
| Affecting multiple systems |
facial (Mobius syndrome, Goldenhar syndrome, Cyclopia, Apert syndrome)
short stature (Aarskog-Scott syndrome, Cockayne syndrome, Cornelia de Lange Syndrome, Dubowitz syndrome, Noonan syndrome, Robinow syndrome, Silver-Russell dwarfism, Seckel syndrome, Smith-Lemli-Opitz syndrome)
limbs (Holt-Oram syndrome, Klippel-Trenaunay-Weber syndrome, Nail-patella syndrome, Rubinstein-Taybi syndrome, Sirenomelia, VACTERL association)
overgrowth (Beckwith-Wiedemann syndrome, Sotos syndrome, Weaver syndrome)
Marfan syndrome - Alport syndrome - Bardet-Biedl syndrome - Zellweger syndrome |
| Other |
spleen: Asplenia - Splenomegaly
endocrine glands: Persistent thyroglossal duct - Thyroglossal cyst
Situs inversus - Conjoined twins
Cowden syndrome - Hamartoma |
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This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "List_of_ICD-9_codes_740-759:_Congenital_anomalies". A list of authors is available in Wikipedia.
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