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6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 associated genes
No signs/symptoms info
Semantic dementia
Maternal uniparental disomy of chromosome 14

C9ORF72 DLK1
CHMP2B MEG3
GRN RTL1
MAPT
PSEN1
VCP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
GRN
(0.74)
DLK1



Citations in the biomedical literature:


Semantic dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP

Maternal uniparental disomy of chromosome 14
DLK1 MEG3 RTL1



Semantic dementia
Maternal uniparental disomy of chromosome 14

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

Synonym(s):
- UPD(14)mat

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- 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:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.