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6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 5
Semantic dementia
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form

C9ORF72 CTNNA3
CHMP2B DSC2
GRN DSG2
MAPT DSP
PSEN1 JUP
VCP LMNA
PKP2
RYR2
TGFB3
TMEM43
TTN


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PSEN1
VCP
PSEN1
VCP
PSEN1
(0.86)
(0.73)
(0.63)
(0.63)
(0.49)
JUP
DSP
DSG2
LMNA
DSP



Citations in the biomedical literature:


Semantic dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP

Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
CTNNA3 DSC2 DSG2 DSP JUP LMNA
PKP2 RYR2 TGFB3 TMEM43 TTN



Semantic dementia
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form

Synonym(s):
- Semantic primary progressive aphasia
- Semantic variant PPA

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: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
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.