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5 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
5 OMIM references -
8 associated genes
No signs/symptoms info
Congenital muscular dystrophy with cerebellar involvement
Familial pancreatic carcinoma

FKRP BRCA1
GMPPB BRCA2
POMGNT1 CDKN2A
POMT1 KRAS
POMT2 MANF
PALB2
SMAD4
TP53


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 pancreatic carcinoma
BRCA1 BRCA2 CDKN2A KRAS MANF PALB2
SMAD4 TP53



Congenital muscular dystrophy with cerebellar involvement
Familial pancreatic carcinoma

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

Synonym(s):
- Familial pancreatic cancer

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic 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:
5 OMIM references -
1 MeSH reference: C535837

No signs/symptoms info available.