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6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
3 OMIM references -
5 associated genes
No signs/symptoms info
Semantic dementia
Autoimmune lymphoproliferative syndrome

C9ORF72 CASP10
CHMP2B FAS
GRN FASLG
MAPT NRAS
PSEN1 PRKCD
VCP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MAPT
VCP
(0.63)
(0.56)
PRKCD
PRKCD



Citations in the biomedical literature:


Semantic dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP

Autoimmune lymphoproliferative syndrome
CASP10 FAS FASLG NRAS PRKCD



Semantic dementia
Autoimmune lymphoproliferative syndrome

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

Synonym(s):
- ALPS
- Canale-Smith syndrome
- FAS deficiency

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare immune disease
- Rare oncologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

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: variable
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
3 OMIM references -
1 MeSH reference: D056735

No signs/symptoms info available.