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Familial renal cell carcinoma
6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial amyloidosis, Finnish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Familial renal cell carcinoma
Familial amyloidosis, Finnish type

DIRC1
(UniProt - OMIM)
 GSN
(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)
FHIT
(0.52)
GSN


Citations in the biomedical literature:


Familial renal cell carcinoma
DIRC1 DIRC2 DIRC3 FHIT HSPBAP1 RNF139

Familial amyloidosis, Finnish type
GSN



Familial renal cell carcinoma
Familial amyloidosis, Finnish type

Synonym(s):
(no synonyms)

Synonym(s):
- Familial amyloid polyneuropathy type 4
- Gelsolin amyloidosis
- Hereditary amyloidosis, Finnish type
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
1 MeSH reference: C536851
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.