ODCs

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

PROTEIN INTERACTIONS: 1

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

Pelizaeus-Merzbacher-like due to HSPD1 mutation

Congenital bilateral absence of vas deferens


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HSPD1	(0.72)	CFTR

Citations in the biomedical literature:

Pelizaeus-Merzbacher-like due to HSPD1 mutation		Congenital bilateral absence of vas deferens
	Synonym(s): - Mitochondrial HSP60 chaperonopathy		Synonym(s): - Congenital bilateral agenesis of vas deferens - Congenital bilateral aplasia of vas deferens

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare infertility - Rare urogenital 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: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: adolescence / young Average age of death: normal Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C535984

No signs/symptoms info available.