ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Adult-onset distal myopathy due to VCP mutation

Familial hypocalciuric hypercalcemia type 1


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	VCP	(0.63)	CASR

Citations in the biomedical literature:

Adult-onset distal myopathy due to VCP mutation		Familial hypocalciuric hypercalcemia type 1
	Synonym(s): (no synonyms)		Synonym(s): - FHH type 1

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537145

No signs/symptoms info available.