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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Spinocerebellar ataxia type 29
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form

ITPR1 CTNNA3
DSC2
DSG2
DSP
JUP
LMNA
PKP2
RYR2
TGFB3
TMEM43
TTN


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ITPR1
(0.52)
RYR2



Citations in the biomedical literature:


Spinocerebellar ataxia type 29
ITPR1
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
CTNNA3 DSC2 DSG2 DSP JUP LMNA
PKP2 RYR2 TGFB3 TMEM43 TTN



Spinocerebellar ataxia type 29
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form

Synonym(s):
- Congenital nonprogressive spinocerebellar ataxia
- SCA29

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

Classification (Orphanet):
- 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:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.