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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant spastic paraplegia type 8
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form

KIAA0196 CTNNA3
DSC2
DSG2
DSP
JUP
LMNA
PKP2
RYR2
TGFB3
TMEM43
TTN


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KIAA0196
(0.63)
LMNA



Citations in the biomedical literature:


Autosomal dominant spastic paraplegia type 8
KIAA0196
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
CTNNA3 DSC2 DSG2 DSP JUP LMNA
PKP2 RYR2 TGFB3 TMEM43 TTN



Autosomal dominant spastic paraplegia type 8
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form

Synonym(s):
- SPG8

Synonym(s):
- Familial isolated arrhythmogenic ventricular cardiomyopathy, left dominant 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: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
1 MeSH reference: C536867
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.