List of ICD-9 codes 740-759: Congenital anomalies
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14. Congenital anomalies (740-759)
nervous system
- (740) Anencephalus and similar anomalies
- (742) Other congenital anomalies of nervous system
eye, ear, face and neck
- (743) Congenital anomalies of eye
- (743.6) Congenital anomalies of eyelids, lacrimal system, and orbit
- (743.4) Coloboma and other anomalies of anterior segment
- (743.45) Aniridia
- (744) Congenital anomalies of ear, face, and neck
- (744.0) Anomalies of ear causing impairment of hearing
- (744.4) Branchial cleft cyst or fistula; preauricular sinus
circulatory system
- (745) Bulbus cordis anomalies and anomalies of cardiac septal closure
- (746) Other congenital anomalies of heart
- (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
- (750) Other congenital anomalies of upper alimentary tract
- (751) Other congenital anomalies of digestive system
genital organs
urinary system
musculoskeletal system
- (754) Certain congenital musculoskeletal deformities
- (754.1) Torticollis, sternomastoid
- (754.3) Dislocation of hip, unilateral
- (754.5) Varus deformities of feet
- (754.6) Valgus deformities of feet
- (754.8) Other specified nonteratogenic anomalies
- (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
- (757) Congenital anomalies of the integument
- (757.3) Other specified anomalies of skin
- (757.32) Birthmarks
- (757.39) Other specified congenital anomalies of skin
- (757.6) Supernumerary nipple
- (757.3) Other specified anomalies of skin
chromosomal anomalies
- (758) Chromosomal anomalies
- (758.0) Down's syndrome
- (758.1) Patau's syndrome
- (758.2) Edward's syndrome
- (758.3) Autosomal deletion syndromes
- (758.4) Balanced autosomal translocation in normal individual
- (758.5) Other conditions due to autosomal anomalies
- (758.6) Gonadal dysgenesis
- (758.7) Klinefelter's syndrome
- (758.8) Other conditions due to sex chromosome anomalies
- (758.9) Conditions due to anomaly of unspecified chromosome
Other
- (759) Other and unspecified congenital anomalies
- (759.5) Tuberous sclerosis
- (759.6) Other congenital hamartoses not elsewhere classified
See also
- List of ICD-9 codes
- ICD-10 Chapter Q: Congenital malformations, deformations and chromosomal abnormalities
- Congenital disorder
Congenital malformations and deformations of nervous system (Q00-Q07, 740-742) | |
|---|---|
| Brain | Anencephaly (Acephaly, Acrania, Iniencephaly) - Encephalocele - Microcephaly - Congenital hydrocephalus (Dandy-Walker syndrome) - other reduction deformities (Holoprosencephaly, Lissencephaly, Pachygyria, Hydranencephaly) - Septo-optic dysplasia - Megalencephaly - Congenital cerebral cysts (Porencephaly, Schizencephaly) - Congenital brain tumors |
| Brain stem | Arnold-Chiari malformation |
| Spinal cord | Spina bifida - Currarino syndrome - Sacrococcygeal teratoma - Diastematomyelia - Syringomyelia |
| see also non-congenital CNS and PNS (G, 320-359) | |
Congenital malformations and deformations of eye, ear, face and neck (Q10-Q18, 743-744) | |
|---|---|
| Eyes | eyelid, lacrimal apparatus and orbit: Ptosis - Ectropion - Entropion - Distichia - Blepharophimosis - Congenital lacrimal duct obstruction
entire eye: Anophthalmia - Microphthalmia lens: Ectopia lentis - Aphakia Aniridia - Axenfeld syndrome - Buphthalmos - Coloboma - Hydrophthalmos - Keratoglobus - Zazam Sheriff Phillips syndrome |
| Ears | Microtia |
| Other face and neck | Otocephaly - Webbed neck - Microstomia - Macrocheilia |
| See also non-congenital eye and ear | |
Congenital malformations and deformations of respiratory system (Q30-Q34, 748) | |
|---|---|
| Nose | Choanal atresia |
| Larynx | Laryngocele - Laryngomalacia |
| Trachea and bronchus | Tracheomalacia |
| Lung | Bronchiectasis - Pulmonary sequestration - Congenital cystic adenomatoid malformation |
| see also non-congenital (J, 460-519) | |
Congenital malformations and deformations of musculoskeletal system (Q65-Q79, 754-756) | |
|---|---|
| Limbs | hip: Dislocation of hip/Hip dysplasia - Upington disease
feet (Club foot, Flat feet, Pes cavus) systemic dislocations Larsen syndrome head, face, spine and chest: skull, face and jaw (Dolichocephaly, Greig cephalopolysyndactyly syndrome, Plagiocephaly) - spine Scoliosis - chest (Pectus excavatum, Pectus carinatum) any combination head, face, jaw, upper limb, lower limb, pelvis, dactyly Antley-Bixler syndrome - Schmitt Gillenwater Kelly syndrome dactyly Polydactyly/Syndactyly (Webbed toes) - Cenani Lenz syndactylism reduction deficits (Acheiropodia, Amelia, Ectrodactyly, Phocomelia) upper limb (Cleidocranial dysostosis, Madelung's deformity, Sprengel's deformity, Wallis Zieff Goldblatt syndrome) knee (Genu valgum, Genu varum) other Arthrogryposis |
| Skull and facial bones | Carpenter syndrome - Craniodiaphyseal dysplasia - Craniosynostosis (Scaphocephaly) - Crouzon syndrome - Hypertelorism - Macrocephaly - Oxycephaly - Platybasia - Saethre-Chotzen syndrome - Treacher Collins syndrome - Trigonocephaly |
| Spine and bony thorax | Klippel-Feil syndrome - Spondylolisthesis - Cervical rib - Bifid rib |
| Osteochondrodysplasia | developement of cartilage, tubular bones and spine: Achondrogenesis/Hypochondrogenesis - Boomerang dysplasia - Thanatophoric dysplasia - Short rib-polydactyly syndrome - Chondrodysplasia punctata (Rhizomelic chondrodysplasia punctata, Conradi-Hünermann syndrome), Achondroplasia (Hypochondroplasia, Osteosclerosis congenita) - Ellis-van Creveld syndrome - Otospondylomegaepiphyseal dysplasia - Spondyloepiphyseal dysplasia congenita - Osteogenesis imperfecta - McCune-Albright syndrome - Osteopetrosis - Metaphyseal dysplasia - Recessive multiple epiphyseal dysplasia - Hereditary multiple exostoses - Osteopoikilosis - Chondrodystrophy - Osteodystrophy - Atelosteogenesis, type II - Diastrophic dysplasia |
| Other | abdominal wall (Congenital diaphragmatic hernia, Omphalocele, Gastroschisis, Prune belly syndrome) - Ehlers-Danlos syndrome |
| See also non-congenital conditions (M, 710-739) | |
Congenital malformations and deformations of integument (Q80-Q84, 757) | |
|---|---|
| Congenital ichthyosis | Epidermolytic hyperkeratosis - Harlequin type ichthyosis - Ichthyosis lamellaris - Ichthyosis vulgaris - Netherton's syndrome - X-linked ichthyosis - Zunich-Kaye syndrome |
| Epidermolysis bullosa | Epidermolysis bullosa simplex - Epidermolysis bullosa dystrophica |
| Other skin disease | Hereditary lymphedema - Mastocytosis - Urticaria pigmentosa - Incontinentia pigmenti - Ectodermal dysplasia - EEM syndrome - Hay-Wells syndrome - Kindler syndrome - Port-wine stain - Cutis laxa - Darier's disease - Pseudoxanthoma elasticum DNA repair-deficiency disorder: Bloom syndrome - Rothmund-Thomson syndrome - Xeroderma pigmentosum |
| Nail disease | Leukonychia - Pachyonychia congenita |
| Malformations of breast | Amastia - Accessory breast - Athelia - Supernumerary nipple - Micromastia |
| Hair disease | Monilethrix - Sabinas brittle hair syndrome |
| see also non-congenital (L, 680-709) | |
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), Trisomy 22, Trisomy 16 |
| 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, Other Karyotypes: XXXX, XXYY, XXXXX, XXXXY |
| Translocations | Philadelphia chromosome, Burkitt's lymphoma |
| Other | Fragile X syndrome, Gonadal dysgenesis (Mixed gonadal dysgenesis) |
Phakomatoses and other congenital malformations not elsewhere classified (Q85-Q89, 759) | |
|---|---|
| Phakomatoses | Abdallat Davis Farrage syndrome - Ataxia telangiectasia - Incontinentia pigmenti - Neurofibromatosis (type I, type II) - Peutz-Jeghers syndrome - Sturge-Weber syndrome - Tuberous sclerosis - Von Hippel-Lindau disease |
| 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 (Adducted thumb syndrome, Holt-Oram syndrome, Klippel-Trenaunay-Weber syndrome, Nail-patella syndrome, Rubinstein-Taybi syndrome, Sirenomelia, VACTERL association) overgrowth (Beckwith-Wiedemann syndrome, Sotos syndrome, Weaver syndrome) combined/other Ablepharon macrostomia syndrome - Alport syndrome - Bardet-Biedl syndrome - Branchio-oto-renal syndrome - Donohue syndrome - Fraser syndrome - Keutel syndrome - Marfan syndrome - Timothy syndrome - Urban-Rogers-Meyer syndrome - Vici syndrome - Yunis-Varon syndrome - Zellweger syndrome - Zimmerman-Laband syndrome - Zori Stalker Williams syndrome |
| Other | spleen: Asplenia - Splenomegaly
endocrine glands: Persistent thyroglossal duct - Thyroglossal cyst Conjoined twins - Cowden syndrome - Hamartoma - Impossible syndrome - Situs inversus |
| ||||
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
