ODCs

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4 OMIM references -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Combined pituitary hormone deficiencies, genetic forms

Familial clubfoot due to 5q31 microdeletion


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	POU1F1	(0.78)	PITX1

Citations in the biomedical literature:

Combined pituitary hormone deficiencies, genetic forms		Familial clubfoot due to 5q31 microdeletion
	Synonym(s): - Familial congenital hypopituitarism - Multiple pituitary hormone deficiencies, genetic forms		Synonym(s): - Hereditary clubfoot due to 5q31 microdeletion

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare infertility		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 4 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.