Search for a rare disease
Other search option(s)
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
Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.