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Congenital alpha2 antiplasmin deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant severe congenital neutropenia
4 OMIM references -
2 associated genes
No signs/symptoms info
Congenital alpha2 antiplasmin deficiency
Autosomal dominant severe congenital neutropenia

SERPINF2
(UniProt - OMIM)
 ELANE
(UniProt - OMIM)
GFI1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SERPINF2
(0.77)
ELANE


Citations in the biomedical literature:


Congenital alpha2 antiplasmin deficiency
SERPINF2
Autosomal dominant severe congenital neutropenia
ELANE GFI1



Congenital alpha2 antiplasmin deficiency
Autosomal dominant severe congenital neutropenia

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:
(no data available)
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.