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1 associated gene
No signs/symptoms info
COMMON GENES: 1
Progeria-associated arthropathy
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form

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


COMMON
GENES
LMNA



Citations in the biomedical literature:


Progeria-associated arthropathy
LMNA
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
CTNNA3 DSC2 DSG2 DSP JUP
PKP2 RYR2 TGFB3 TMEM43 TTN



Progeria-associated arthropathy
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form

Synonym(s):
(no synonyms)

Synonym(s):
- Familial isolated arrhythmogenic ventricular cardiomyopathy, classic form
- Familial isolated arrhythmogenic ventricular cardiomyopathy, right dominant form
- Familial isolated arrhythmogenic ventricular dysplasia, classic form

Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the circulatory system -

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

External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.