thrombomodulin anomalies, familial

Preferred Label : thrombomodulin anomalies, familial;

Origin ID

C536900;

UMLS CUI

C2931365;

Currated CISMeF NLP mapping
- Familial thrombomodulin anomalies [ORDO Disease]
- Familial thrombomodulin anomalies (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- thrombophilia [MeSH Descriptor]
ORDO relation(s)
- Familial thrombomodulin anomalies [ORDO Disease]
Record concept(s)
- Thrombomodulin anomalies, familial [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial thrombomodulin anomalies [ORDO Disease]
- Familial thrombomodulin anomalies (disorder) [SNOMED CT concept]