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: -

Summary

This disease is described under Familial clubfoot with or without associated lower limb anomalies

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