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5 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Congenital muscular dystrophy with cerebellar involvement
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form

FKRP CTNNA3
GMPPB DSC2
POMGNT1 DSG2
POMT1 DSP
POMT2 JUP
LMNA
PKP2
RYR2
TGFB3
TMEM43
TTN


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
GMPPB
GMPPB
(0.63)
(0.63)
JUP
LMNA



Citations in the biomedical literature:


Congenital muscular dystrophy with cerebellar involvement
FKRP GMPPB POMGNT1 POMT1 POMT2
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
CTNNA3 DSC2 DSG2 DSP JUP LMNA
PKP2 RYR2 TGFB3 TMEM43 TTN



Congenital muscular dystrophy with cerebellar involvement
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form

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

Synonym(s):
- Familial isolated arrhythmogenic ventricular cardiomyopathy, biventricular form

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease

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

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
5 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.