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1 OMIM reference -
7 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Translocation renal cell carcinoma
Juvenile Huntington disease

ASPSCR1 HTT
CLTC
NONO
PRCC
SFPQ
TFE3
TFEB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CLTC
(0.84)
HTT



Citations in the biomedical literature:


Translocation renal cell carcinoma
ASPSCR1 CLTC NONO PRCC SFPQ TFE3
TFEB
Juvenile Huntington disease
HTT



Translocation renal cell carcinoma
Juvenile Huntington disease

Synonym(s):
- Carcinoma associated with MITF/TFE translocation
- Translocation carcinoma

Synonym(s):
- JHD
- Juvenile Huntington chorea

Classification (Orphanet):
- Rare oncologic disease
- Rare renal disease
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: 1-9 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.