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Semantic dementia
6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary motor and sensory neuropathy type 5
1 OMIM reference -
1 associated gene
No signs/symptoms info
Semantic dementia
Hereditary motor and sensory neuropathy type 5

C9ORF72
(UniProt - OMIM)
 MFN2
(UniProt - OMIM)
CHMP2B
(UniProt - OMIM)
GRN
(UniProt - OMIM)
MAPT
(UniProt - OMIM)
PSEN1
(UniProt - OMIM)
VCP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
VCP
(0.63)
MFN2


Citations in the biomedical literature:


Semantic dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP

Hereditary motor and sensory neuropathy type 5
MFN2



Semantic dementia
Hereditary motor and sensory neuropathy type 5

Synonym(s):
- Semantic primary progressive aphasia
- Semantic variant PPA
Synonym(s):
- Charcot-Marie-Tooth disease - pyramidal features
- HMSN 5
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:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.