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Pelizaeus-Merzbacher-like due to HSPD1 mutation
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial renal cell carcinoma
6 associated genes
No signs/symptoms info
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Familial renal cell carcinoma

HSPD1
(UniProt - OMIM)
 DIRC1
(UniProt - OMIM)
DIRC2
(UniProt - OMIM)
DIRC3
(UniProt - OMIM)
FHIT
(UniProt - OMIM)
HSPBAP1
(UniProt - OMIM)
RNF139
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HSPD1
(0.85)
FHIT


Citations in the biomedical literature:


Pelizaeus-Merzbacher-like due to HSPD1 mutation
HSPD1
Familial renal cell carcinoma
DIRC1 DIRC2 DIRC3 FHIT HSPBAP1 RNF139



Pelizaeus-Merzbacher-like due to HSPD1 mutation
Familial renal cell carcinoma

Synonym(s):
- Mitochondrial HSP60 chaperonopathy
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
(no data available)
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:
No OMIM references
1 MeSH reference: C536851
No signs/symptoms info available.