anti-plasmin deficiency, congenital

Preferred Label : anti-plasmin deficiency, congenital;

CISMeF synonym : antiplasmin deficiency;

MeSH synonym : antiplasmin deficiency, congenital;

Related MeSH term : Alpha-2-plasmin inhibitor deficiency; Plasmin Inhibitor Deficiency;

Details

Origin ID

C537777;

UMLS CUI

C3489734;

Automatic exact mappings (from CISMeF team)
- Alpha-2-antiplasmin deficiency (disorder) [SNOMED CT concept]
- Alpha-2-plasmin inhibitor deficiency [OMIM Phenotype]
- Congenital alpha-2-antiplasmin deficiency (disorder) [SNOMED CT concept]
- alpha-2-plasmin inhibitor deficiency [DO Concept]
CISMeF manual mappings
- Congenital alpha2-antiplasmin deficiency [ORDO Disease]
Has phenotype(s) (HPO)
- Spontaneous joint hemorrhage [HPO term]
MeSH term(s) associated for indexing
- alpha-2-Antiplasmin [MeSH Descriptor]
- hemorrhagic disorders [MeSH Descriptor]
Record concept(s)
- anti-plasmin deficiency, congenital [MeSH concept]
- antiplasmin deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital alpha2-antiplasmin deficiency [ORDO Disease]

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