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Autosomal recessive spastic paraplegia type 20
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Translocation renal cell carcinoma
1 OMIM reference -
7 associated genes
No signs/symptoms info
Autosomal recessive spastic paraplegia type 20
Translocation renal cell carcinoma

SPG20
(UniProt - OMIM)
 ASPSCR1
(UniProt - OMIM)
CLTC
(UniProt - OMIM)
NONO
(UniProt - OMIM)
PRCC
(UniProt - OMIM)
SFPQ
(UniProt - OMIM)
TFE3
(UniProt - OMIM)
TFEB
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SPG20
(0.72)
CLTC


Citations in the biomedical literature:


Autosomal recessive spastic paraplegia type 20
SPG20
Translocation renal cell carcinoma
ASPSCR1 CLTC NONO PRCC SFPQ TFE3
TFEB



Autosomal recessive spastic paraplegia type 20
Translocation renal cell carcinoma

Synonym(s):
- Childhood-onset spastic paraparesis - distal muscle wasting
- SPG20
- Troyer syndrome
Synonym(s):
- Carcinoma associated with MITF/TFE translocation
- Translocation carcinoma
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare oncologic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.