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6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
5 OMIM references -
3 associated genes
No signs/symptoms info
Semantic dementia
Periventricular nodular heterotopia

C9ORF72 ARFGEF2
CHMP2B ERMARD
GRN FLNA
MAPT
PSEN1
VCP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PSEN1
VCP
(0.89)
(0.63)
FLNA
ARFGEF2



Citations in the biomedical literature:


Semantic dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP

Periventricular nodular heterotopia
ARFGEF2 ERMARD FLNA



Semantic dementia
Periventricular nodular heterotopia

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

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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: -
Average age of death: -
Type of inheritance: autosomal recessive

External references:
No OMIM references
No MeSH references
External references:
5 OMIM references -
1 MeSH reference: D054091

No signs/symptoms info available.