ODCs

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

PROTEIN INTERACTIONS: 1

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

Pelizaeus-Merzbacher-like due to HSPD1 mutation

Hereditary breast cancer


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HSPD1	(0.75)	BRCA1

Citations in the biomedical literature:

Pelizaeus-Merzbacher-like due to HSPD1 mutation		Hereditary breast cancer
	Synonym(s): - Mitochondrial HSP60 chaperonopathy		Synonym(s): - Familial breast cancer - Familial breast carcinoma - Hereditary breast carcinoma

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare gynecologic or obstetric disease - Rare oncologic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Neoplasms -

	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: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: 6 OMIM references - No MeSH references

No signs/symptoms info available.