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Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Semantic dementia
6 associated genes
No signs/symptoms info
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Semantic dementia

ISG15
(UniProt - OMIM)
 C9ORF72
(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)
ISG15
(0.63)
VCP


Citations in the biomedical literature:


Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
ISG15
Semantic dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP



Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Semantic dementia

Synonym(s):
- MSMD due to complete ISG15 deficiency
Synonym(s):
- Semantic primary progressive aphasia
- Semantic variant PPA
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.