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LD2F.1 Syndromes with multiple structural anomalies, not of environmental origin

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

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• 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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