Orphanet: Ulnar/fibula ray defect brachydactyly syndrome

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Ulnar/fibula ray defect-brachydactyly syndrome

Disease definition

Ulnar/fibula ray defect - brachydactyly syndrome is a very rare malformation syndrome characterized by ulnar hypoplasia associated with hypoplastic to absent fourth and/or fifth digits, fibular hypoplasia, short stature and facial dysmorphism.


Classification level: Disorder
  • Synonym(s):
    • Morava-Mehes syndrome
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Infancy, Neonatal
  • ICD-10: Q73.8
  • OMIM: 608571
  • UMLS: C1837830
  • MeSH: -
  • GARD: -
  • MedDRA: -

Detailed information


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