Thrombomodulin anomalies, familial

Preferred Label : Thrombomodulin anomalies, familial;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0531361;

UMLS CUI

C2931365;

Currated CISMeF NLP mapping
- Familial thrombomodulin anomalies [ORDO Disease]
- Familial thrombomodulin anomalies (disorder) [SNOMED CT concept]
Related record
- thrombomodulin anomalies, familial [MeSH Supplementary 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]