LD26.1 Complex brachydactylies

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2025-01

A disease caused by failure of the digits to correctly develop during the antenatal period. This disease is characterised by multiple digits of below normal length. This condition may be associated with mutation in the GDF5 gene.

exclusions

• Catel-Manzke syndrome  (LD2F.1)

postcoordination

synonyms

• Complex brachydactylies
• Brachydactyly type A1
• Brachydactyly type A2
• Brachydactyly type A3
• Brachydactyly type A4
• Brachydactyly type A5
• Brachydactyly type A6
• Brachydactyly type A7
• Brachydactyly type B
• Brachydactyly type B2
• Brachydactyly type C
• Brachydactyly type D
• Brachydactyly type E
• Ballard syndrome
• Brachydactyly types B and E combined
• Pitt-Williams brachydactyly
• Brachydactyly-elbow wrist dysplasia

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