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6 associated genes
No signs/symptoms info
COMMON GENES: 6
PROTEIN INTERACTIONS: 1
1 OMIM reference -
6 associated genes
No signs/symptoms info
Semantic dementia
Behavioral variant of frontotemporal dementia

C9ORF72 C9ORF72
CHMP2B CHMP2B
GRN GRN
MAPT MAPT
PSEN1 PSEN1
VCP VCP


COMMON
GENES
C9ORF72
CHMP2B
GRN
MAPT
PSEN1
VCP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MAPT
(0.55)
PSEN1



Citations in the biomedical literature:


Semantic dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP

Behavioral variant of frontotemporal dementia




Semantic dementia
Behavioral variant of frontotemporal dementia

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

Synonym(s):
- bv-FTD

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

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

Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.