Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
6 associated genes
No signs/symptoms info
Autosomal dominant spastic paraplegia type 13
Familial renal cell carcinoma

HSPD1 DIRC1
DIRC2
DIRC3
FHIT
HSPBAP1
RNF139


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HSPD1
(0.85)
FHIT



Citations in the biomedical literature:


Autosomal dominant spastic paraplegia type 13
HSPD1
Familial renal cell carcinoma
DIRC1 DIRC2 DIRC3 FHIT HSPBAP1 RNF139



Autosomal dominant spastic paraplegia type 13
Familial renal cell carcinoma

Synonym(s):
- SPG13

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
1 MeSH reference: C537485
External references:
No OMIM references
1 MeSH reference: C536851

No signs/symptoms info available.