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5 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
6 OMIM references -
4 associated genes
No signs/symptoms info
Congenital muscular dystrophy with cerebellar involvement
Hereditary breast cancer

FKRP BRCA1
GMPPB BRCA2
POMGNT1 KLLN
POMT1 XRCC2
POMT2


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
Hereditary breast cancer
BRCA1 BRCA2 KLLN XRCC2



Congenital muscular dystrophy with cerebellar involvement
Hereditary breast cancer

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

Synonym(s):
- Familial breast cancer
- Familial breast carcinoma
- Hereditary breast carcinoma

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare oncologic 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:
6 OMIM references -
No MeSH references

No signs/symptoms info available.