Orphanet: Familial clubfoot due to PITX1 point mutation
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Familial clubfoot due to PITX1 point mutation

ORPHA:293150

Classification level: Subtype of disorder
  • Synonym(s):
    • Hereditary clubfoot due to PITX1 point mutation
  • Prevalence: -
  • Inheritance: -
  • Age of onset: -
  • ICD-10: Q66.8
  • OMIM: 119800
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -
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