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6 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
3 OMIM references -
3 associated genes
No signs/symptoms info
Semantic dementia
Frontotemporal dementia with motor neuron disease

C9ORF72 C9ORF72
CHMP2B FUS
GRN TARDBP
MAPT
PSEN1
VCP


COMMON
GENES
C9ORF72


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
VCP
(0.73)
TARDBP



Citations in the biomedical literature:


Semantic dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP

Frontotemporal dementia with motor neuron disease
FUS TARDBP



Semantic dementia
Frontotemporal dementia with motor neuron disease

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

Synonym(s):
- FTD-ALS
- FTD-MND
- Frontotemporal dementia with amyotrophic lateral sclerosis

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):
(no data available)

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: adult
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
3 OMIM references -
No MeSH references

No signs/symptoms info available.