autosomal dominant deficiency of plasminogen

Preferred Label : autosomal dominant deficiency of plasminogen;

Origin ID

DC-65424;

UMLS CUI

C0521806;

Currated CISMeF NLP mapping
- Autosomal dominant deficiency of plasminogen (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Hereditary deficiency of other clotting factors [ICD-10 Sub-category (who)]
Metaterm(s)
- hematology [CISMeF Metaterm]
SNOMED CT concept
- Autosomal dominant deficiency of plasminogen (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant deficiency of plasminogen (disorder) [SNOMED CT concept]