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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
19 OMIM references -
12 associated genes
No signs/symptoms info
Autosomal dominant spastic paraplegia type 13
Familial prostate cancer

HSPD1 BRCA1
BRCA2
CHEK2
ELAC2
EPHB2
HNF1B
HOXB13
MSMB
MSR1
NBN
RNASEL
SRD5A2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HSPD1
(0.75)
BRCA1



Citations in the biomedical literature:


Autosomal dominant spastic paraplegia type 13
HSPD1
Familial prostate cancer
BRCA1 BRCA2 CHEK2 ELAC2 EPHB2 HNF1B
HOXB13 MSMB MSR1 NBN RNASEL SRD5A2



Autosomal dominant spastic paraplegia type 13
Familial prostate cancer

Synonym(s):
- SPG13

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
- Rare urogenital disease

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:
19 OMIM references -
1 MeSH reference: C537243

No signs/symptoms info available.