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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
6 associated genes
No signs/symptoms info
Chuvash erythrocytosis
Familial renal cell carcinoma

VHL DIRC1
DIRC2
DIRC3
FHIT
HSPBAP1
RNF139


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
VHL
(0.65)
RNF139



Citations in the biomedical literature:


Chuvash erythrocytosis
VHL
Familial renal cell carcinoma
DIRC1 DIRC2 DIRC3 FHIT HSPBAP1 RNF139



Chuvash erythrocytosis
Familial renal cell carcinoma

Synonym(s):
- Chuvash polycythemia
- Von Hippel-Lindau-dependent polycythemia

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
(no data available)

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
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.