Syndromes with multiple structural anomalies, not of environmental origin
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
code elsewhere
- Fraser syndrome (LD2H.0)
- Waardenburg-Shah syndrome (LD2H.3)
- Oculocerebrorenal syndrome (5C60.0)
- Albinism - black lock - cell migration disorder of the neurocytes of the gut - sensorineural deafness (LD2H.Y)
- Bardet-Biedl syndrome (5A61.0)
- Blepharocheilodontic syndrome (LD27.0Y)
- Cat-eye syndrome (LD41.P)
- Cataract - intellectual deficit - hypogonadism (5A61.0)
- CHARGE syndrome (5A61.0)
- Coffin-Siris syndrome (LD27.0Y)
- Dubowitz syndrome (LD27.0Y)
- Ectodermal dysplasia - ectrodactyly - macular dystrophy (LD27.0Y)
- Ectrodactyly - ectodermal dysplasia - cleft lip or palate (LD27.0Y)
- Ectrodactyly - ectodermal dysplasia without clefting (LD27.0Y)
- Hirschsprung disease - deafness - polydactyly (LD2H.Y)
- Limb-mammary syndrome (LD27.0Y)
- Marshall syndrome (LD27.0Y)
- MODY 5 syndrome (5A13.6)
- Nijmegen breakage syndrome-like disorder (4A01.31)
- Papillorenal syndrome (LA13.7Y)
- Perrault syndrome (LD2H.Y)
- Phocomelia - ectrodactyly - deafness - sinus arrhythmia (LD2H.Y)
- Shwachman-Diamond syndrome (3A70.0)
- Smith-Magenis syndrome (LD44.H1)
- Split hand - split foot - deafness (LD2H.Y)
- Triple A syndrome (5A74.Y)
- Waardenburg syndrome (EC23.2Y)
- WAGR syndrome (LD2A.Y)
- Williams-Beuren syndrome (LD44.70)
- Gorham-Stout disease (FB86.2)
- Alagille syndrome (LB20.0Y)
- Deafness – onychodystrophy (LD27.0Y)
- Autosomal recessive cutis laxa, type 3 (LD28.2)
- Macrocephaly – alopecia – cutis laxa – scoliosis syndrome (LD28.2)
- SCARF syndrome (LD28.2)
- Lethal restrictive dermopathy (EE6Y)
- Encephalocraniocutaneous lipomatosis (EF02.1)
- Dahlberg-Borer-Newcomer syndrome (LD27.0Y)
sections/codes in this section (LD2F.1-LD2F.1)
- Prune belly syndrome (LD2F.10)
- VATER association (LD2F.11)
- Sirenomelia (LD2F.12)
- Meckel-Gruber syndrome (LD2F.13)
- MURCS association (LD2F.14)
- Noonan syndrome (LD2F.15)
- Otomandibular dysplasia (LD2F.16)
- Other specified syndromes with multiple structural anomalies, not of environmental origin (LD2F.1Y)
- Syndromes with multiple structural anomalies, not of environmental origin, unspecified (LD2F.1Z)
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