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5 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
19 OMIM references -
12 associated genes
No signs/symptoms info
Congenital muscular dystrophy with cerebellar involvement
Familial prostate cancer

FKRP BRCA1
GMPPB BRCA2
POMGNT1 CHEK2
POMT1 ELAC2
POMT2 EPHB2
HNF1B
HOXB13
MSMB
MSR1
NBN
RNASEL
SRD5A2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
POMGNT1
(0.63)
BRCA1



Citations in the biomedical literature:


Congenital muscular dystrophy with cerebellar involvement
FKRP GMPPB POMGNT1 POMT1 POMT2
Familial prostate cancer
BRCA1 BRCA2 CHEK2 ELAC2 EPHB2 HNF1B
HOXB13 MSMB MSR1 NBN RNASEL SRD5A2



Congenital muscular dystrophy with cerebellar involvement
Familial prostate cancer

Synonym(s):
- CMD with cerebellar involvement
- CMD-CRB

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Inborn errors of metabolism
- 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:
(no data available)
Epidemiological data:
(no data available)

External references:
5 OMIM references -
No MeSH references
External references:
19 OMIM references -
1 MeSH reference: C537243

No signs/symptoms info available.