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Congenital factor VII deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Semantic dementia
6 associated genes
No signs/symptoms info
Congenital factor VII deficiency
Semantic dementia

F7
(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)
F7
(0.63)
VCP


Citations in the biomedical literature:


Congenital factor VII deficiency
F7
Semantic dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP



Congenital factor VII deficiency
Semantic dementia

Synonym(s):
- Congenital proconvertin deficiency
- Hypoproconvertinemia
Synonym(s):
- Semantic primary progressive aphasia
- Semantic variant PPA
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic 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: 1-9 / 1 000 000
Average age onset: variable
Average age of death: -
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:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.