Orphanet: Acrocephalosyndactyly

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Disease definition

A rare group of inherited congenital malformation disorders characterized by craniosynostosis and fusion or webbing of the fingers or toes, often with other associated manifestations.


Classification level: Group of disorders
  • Synonym(s):
    • ACS
    • Acrocephalosyndactylia
  • Prevalence: Unknown
  • Inheritance: Autosomal dominant or Not applicable 
  • Age of onset: Neonatal, Antenatal
  • ICD-10: Q87.0
  • OMIM: -
  • UMLS: C1510455
  • MeSH: D000168
  • GARD: -
  • MedDRA: 10000590

Detailed information


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