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Congenital alpha2 antiplasmin deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital factor XIII deficiency
2 OMIM references -
2 associated genes
No signs/symptoms info
Congenital alpha2 antiplasmin deficiency
Congenital factor XIII deficiency

SERPINF2
(UniProt - OMIM)
 F13A1
(UniProt - OMIM)
F13B
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SERPINF2
(0.52)
F13A1


Citations in the biomedical literature:


Congenital alpha2 antiplasmin deficiency
SERPINF2
Congenital factor XIII deficiency
F13A1 F13B



Congenital alpha2 antiplasmin deficiency
Congenital factor XIII deficiency

Synonym(s):
(no synonyms)

Synonym(s):
- Fibrin-stabilizing factor deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic 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: variable
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.