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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
2 associated genes
No signs/symptoms info
Congenital factor V deficiency
Autosomal dominant severe congenital neutropenia

F5 ELANE
GFI1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
F5
(0.52)
ELANE



Citations in the biomedical literature:


Congenital factor V deficiency
F5
Autosomal dominant severe congenital neutropenia
ELANE GFI1



Congenital factor V deficiency
Autosomal dominant severe congenital neutropenia

Synonym(s):
- Owren disease
- Parahemophilia
- Proaccelerin deficiency

Synonym(s):
(no synonyms)

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

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

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
4 OMIM references -
No MeSH references

No signs/symptoms info available.