congenital plasminogen deficiency

Preferred Label : congenital plasminogen deficiency;

MeSH synonym : hypoplasminogenemia;

Is substance : O;

Origin ID

C580017;

UMLS CUI

C0398621;

Automatic exact mappings (from CISMeF team)
- Decreased level of plasminogen [HPO term]
- plasminogen deficiency type I [DO Concept]
Currated CISMeF NLP mapping
- Hypoplasminogenemia [PASCAL descriptor]
- Hypoplasminogenemia [ORDO Disease]
- Hypoplasminogenemia (disorder) [SNOMED CT concept]
- hypoplasminogenemia [SNOMED Notion]
- hypoplasminogenemia [Disease (Nov.)]
DO Cross reference
- plasminogen deficiency type I [DO Concept]
MeSH term(s) associated for indexing
- coagulation protein disorders [MeSH Descriptor]
Record concept(s)
- congenital plasminogen deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypoplasminogenemia [ORDO Disease]
- Hypoplasminogenemia [PASCAL descriptor]
- Hypoplasminogenemia (disorder) [SNOMED CT concept]
- hypoplasminogenemia [SNOMED Notion]
- hypoplasminogenemia [Disease (Nov.)]