List_of_ICD-9_codes_740-759:_Congenital

List of ICD-9 codes 740-759: Congenital anomalies

Contents

1 14. Congenital anomalies (740-759)

1.1 nervous system

1.2 eye, ear, face and neck

1.3 circulatory system

1.4 respiratory system

1.5 digestive system

1.6 genital organs

1.7 urinary system

1.8 musculoskeletal system

1.9 integument

1.10 chromosomal anomalies

1.11 Other

2 See also

14. Congenital anomalies (740-759)

(755) Other congenital anomalies of limbs
- (755.0) Polydactyly
- (755.5) Other congenital anomalies of upper limb including shoulder girdle
  - (755.55) Acrocephalosyndactyly
    - Apert syndrome
- (755.9) Limb anomaly, unspec.

(756) Other congenital musculoskeletal anomalies
- (756.1) Anomalies of spine
  - (756.12) Spondylolisthesis
  - (756.17) Spina bifida occulta
- (756.5) Osteodystrophies
  - (756.51) Osteogenesis imperfecta

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

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
  - (758.31) Cri du chat
  - (758.32) Velo-cardio-facial syndrome
  - (758.33) Other microdeletions
    - Miller-Dieker syndrome
    - Smith-Magenis syndrome
- (758.4) Balanced autosomal translocation in normal individual
- (758.5) Other conditions due to autosomal anomalies
- (758.6) Gonadal dysgenesis
  - Turner's syndrome
  - XO syndrome
- (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
  - (759.82) Marfan syndrome
- (759.6) Other congenital hamartoses not elsewhere classified
  - Cowden syndrome

v • d • e 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 Polymicrogyria (Bilateral frontoparietal polymicrogyria)

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)

v • d • e

Congenital malformations and deformations of eyes (Q10-Q15, 743)

Adnexa

Eyelid	Ptosis - Ectropion - Entropion - Distichia - Blepharophimosis - Ablepharon

Lacrimal apparatus	Congenital lacrimal duct obstruction

Eyeball

Entire eye	Anophthalmia - Microphthalmia

Lens	Ectopia lentis - Aphakia

Iris	Aniridia

Anterior segment	Axenfeld syndrome

Other	Buphthalmos - Coloboma - Hydrophthalmos - Keratoglobus - Norrie disease

See also non-congenital

v • d • e Congenital malformations and deformations of ear, face and neck (Q16-Q18, 744)

Ears	Microtia - Low-set ears

Other/combinations	Otocephaly - Hallermann-Streiff syndrome - Webbed neck - Microstomia - Macrocheilia

See also non-congenital

v • d • e

Congenital malformations and deformations of circulatory system (Q20-Q24, 745-746)

Heart
(R→L, L→R)

Cardiac chambers
and connections

Persistent truncus arteriosus - Double outlet right ventricle (Taussig-Bing syndrome) - Transposition of the great vessels (dextro, levo) - Brugada syndrome

Cardiac septa

Ventricular septal defect - Atrial septal defect (Lutembacher's syndrome) - Atrioventricular septal defect (Ostium primum) - Tetralogy of Fallot - Eisenmenger's syndrome

Valvular heart disease/
heart chambers

Right	pulmonary valves (stenosis, insufficiency) - tricuspid valves (stenosis, atresia, Ebstein's anomaly)

Left	aortic valves (stenosis, insufficiency, bicuspid) - mitral valves (stenosis, regurgitation) - Hypoplastic left heart syndrome

Other

Dextrocardia - Levocardia - Cor triatriatum - Crisscross heart

See also non-congenital, neoplasia

v • d • e

Congenital malformations and deformations of respiratory system (Q30-Q34, 748)

Upper RT

Nose	Choanal atresia

Larynx	Laryngocele - Laryngomalacia

Lower RT

Trachea and bronchus	Tracheomalacia - Tracheal stenosis - Bronchomalacia - Mounier-Kuhn syndrome

Lung	Bronchiectasis - Pulmonary sequestration - Congenital cystic adenomatoid malformation

see also non-congenital, tumors

v • d • e

Congenital malformations and deformations of digestive system (Q35-Q45, 749-751)

Upper GI tract

Tongue, mouth and pharynx	Cleft lip and palate - Van der Woude syndrome - tongue (Ankyloglossia, Macroglossia, Hypoglossia) - Pharyngeal pouch

Esophagus	Esophageal atresia - Tracheoesophageal fistula - esophageal rings (Esophageal web - upper, Schatzki ring - lower)

Stomach	Pyloric stenosis - Hiatus hernia

Lower GI tract

Intestines	Intestinal atresia (Duodenal atresia) - Meckel's diverticulum - Hirschsprung's disease - Intestinal malrotation - Dolichocolon

Rectum/anus	Imperforate anus - Persistent cloaca

Accessory

Pancreas	Annular pancreas - Accessory pancreas - Pancreas divisum

Bile duct	Choledochal cysts (Caroli disease) - Biliary atresia

Liver	Alagille syndrome

See also non-congenital, neoplasia, symptoms/signs

v • d • e

Congenital malformations and deformations of genital organs (Q50-Q56, 752)

Female

Uterine malformation	Mullerian agenesis, Unicornuate uterus, Uterus didelphys, Bicornuate uterus, Uterine septum, Arcuate uterus

Other	Vaginal septum - Clitoromegaly

Male

Testicle	Cryptorchidism, Polyorchidism, Monorchism, Anorchia

Penis	Hypospadias, Chordee, Micropenis, Macropenis, Penile agenesis, Diphallia

SDS

Pseudohermaphroditism - True hermaphroditism - Mixed gonadal dysgenesis - Swyer syndrome - Persistent Mullerian duct syndrome

See also noncongenital, neoplasia

v • d • e

Congenital malformations and deformations of urinary system (Q60-Q64, 753)

Abdominal

Kidney	Renal agenesis/Potter syndrome, Papillorenal syndrome cystic (Polycystic kidney disease, Meckel syndrome, Multicystic dysplastic kidney, Medullary sponge kidney) Horseshoe kidney - Renal ectopia - Nephronophthisis

Ureter	Ectopic ureter - Megaureter

Pelvic

Bladder	Bladder exstrophy

Urethra	Epispadias

Vestigial

Urachus

Urachal cyst

See also non-congenital, neoplasia, symptoms/signs

v • d • e

Congenital malformations and deformations of musculoskeletal system / musculoskeletal abnormality (Q65-Q76, 754-756)

Limb/
dysmelia

Upper	Cleidocranial dysostosis - Madelung's deformity - Sprengel's deformity - Wallis Zieff Goldblatt syndrome - Clinodactyly

Lower	hip: Dislocation of hip/Hip dysplasia - Upington disease - Coxa valga - Coxa vara knee: Genu valgum - Genu varum feet: Club foot - Flat feet - Pes cavus

Either/both	dactyly: Polydactyly/Syndactyly (Webbed toes) - Arachnodactyly - Cenani Lenz syndactylism reduction deficits: Acheiropodia - Amelia - Ectrodactyly - Phocomelia - Brachydactyly multiple joints: Arthrogryposis - Larsen syndrome - Rapadilino syndrome

Craniofacial

Craniosynostosis: Scaphocephaly - Oxycephaly - Trigonocephaly

Craniofacial dysostosis: Crouzon syndrome - Hypertelorism - Hallermann-Streiff syndrome - Treacher Collins syndrome

other: Macrocephaly - Platybasia - Craniodiaphyseal dysplasia - Dolichocephaly - Greig cephalopolysyndactyly syndrome - Plagiocephaly - Saddle nose

Other axial

spine: spinal curvature (Scoliosis) - Klippel-Feil syndrome - Spondylolisthesis

ribs: Cervical rib - Bifid rib

sternum: Pectus excavatum - Pectus carinatum

Abdominal wall

Congenital diaphragmatic hernia - Omphalocele - Gastroschisis - Prune belly syndrome

see also non-congenital, neoplasia

v • d • e Osteochondrodysplasia (Q77-Q78, 756.4-756.5)

Osteodysplasia/ osteodystrophy	Osteosclerosis (Raine syndrome) - Osteopoikilosis - Osteopetrosis - Boomerang dysplasia - Hereditary multiple exostoses - Otospondylomegaepiphyseal dysplasia - Fibrous dysplasia (McCune-Albright syndrome)

Chondrodysplasia/ chondrodystrophy	Achondrogenesis/Hypochondrogenesis - Chondrodysplasia punctata (Rhizomelic chondrodysplasia punctata, Conradi-Hünermann syndrome) - Achondroplasia (Hypochondroplasia)

Both/ungrouped	Thanatophoric dysplasia - Short rib-polydactyly syndrome - Ellis-van Creveld syndrome - Spondyloepiphyseal dysplasia congenita - Metaphyseal dysplasia - Multiple epiphyseal dysplasia (Recessive) - Atelosteogenesis, type II - Diastrophic dysplasia - Camurati-Engelmann disease - Antley-Bixler syndrome - Skeletal dysplasia

Collagen diseases	Osteogenesis imperfecta - Ehlers-Danlos syndrome

See also osteochondropathy, neoplasia

v • d • e

Congenital malformations and deformations of integument (Q80-Q84, 757)

Skin disease

Congenital ichthyosis	Epidermolytic hyperkeratosis - Harlequin type ichthyosis - Ichthyosis lamellaris - Ichthyosis vulgaris - Netherton syndrome - X-linked ichthyosis - Zunich-Kaye syndrome

Epidermolysis bullosa	Epidermolysis bullosa simplex - Epidermolysis bullosa dystrophica

Pigmentation disorder	Incontinentia pigmenti - Urticaria pigmentosa

DNA repair-deficiency disorder	Bloom syndrome - Rothmund-Thomson syndrome - Xeroderma pigmentosum

Ectodermal dysplasia	Naegeli syndrome/Dermatopathia pigmentosa reticularis - Hay-Wells syndrome - Hypohidrotic ectodermal dysplasia - Focal dermal hypoplasia

Elastic fiber/Connective tissue	Cutis laxa - Pseudoxanthoma elasticum

Hyperkeratosis/keratinopathy	Meleda disease - Keratosis pilaris - Darier's disease - Dyskeratosis congenita

Other	Familial cutaneous papillomatosis - Kindler syndrome - Port-wine stain - cadherin (EEM syndrome) - immune system (Hereditary lymphedema, Mastocytosis) - Hailey Hailey - Birthmark

Skin appendages

Nail disease

Leukonychia -