ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

1 associated gene
No signs/symptoms info

Familial clubfoot due to PITX1 point mutation

Familial clubfoot due to 5q31 microdeletion

Citations in the biomedical literature:

Familial clubfoot due to PITX1 point mutation		Familial clubfoot due to 5q31 microdeletion
	Synonym(s): - Hereditary clubfoot due to PITX1 point mutation		Synonym(s): - Hereditary clubfoot due to 5q31 microdeletion

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.