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Clear cell renal carcinoma
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal recessive axonal neuropathy with neuromyotonia
1 OMIM reference -
1 associated gene
No signs/symptoms info
Clear cell renal carcinoma
Autosomal recessive axonal neuropathy with neuromyotonia

MITF
(UniProt - OMIM)
 HINT1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MITF
(0.72)
HINT1


Citations in the biomedical literature:


Clear cell renal carcinoma
MITF
Autosomal recessive axonal neuropathy with neuromyotonia
HINT1



Clear cell renal carcinoma
Autosomal recessive axonal neuropathy with neuromyotonia

Synonym(s):
- CCRCC
- Clear cell adenocarcinoma
- Clear cell renal cell adenocarcinoma
- Clear cell renal cell carcinoma
Synonym(s):
- ARAN-NM
- ARCMT2-NM
- Autosomal recessive Charcot-Marie-Tooth disease type 2 with neuromyotonia
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.