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Familial renal cell carcinoma
6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Recessive intellectual disability - motor dysfunction - multiple joint contractures
1 associated gene
No signs/symptoms info
Familial renal cell carcinoma
Recessive intellectual disability - motor dysfunction - multiple joint contractures

DIRC1
(UniProt - OMIM)
 ERLIN2
(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)
RNF139
(0.63)
ERLIN2


Citations in the biomedical literature:


Familial renal cell carcinoma
DIRC1 DIRC2 DIRC3 FHIT HSPBAP1 RNF139

Recessive intellectual disability - motor dysfunction - multiple joint contractures
ERLIN2



Familial renal cell carcinoma
Recessive intellectual disability - motor dysfunction - multiple joint contractures

Synonym(s):
(no synonyms)

Synonym(s):
- IDMDC
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
1 MeSH reference: C536851
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.