congenital thrombotic thrombocytopenic purpura

Preferred Label : congenital thrombotic thrombocytopenic purpura;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0500607;

UMLS CUI

C1268935;

Automatic exact mappings (from CISMeF team)
- Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency [ICD-11 More detail]
Currated CISMeF NLP mapping
- Congenital Thrombotic Thrombocytopenic Purpura [NCIt concept]
- Congenital thrombotic thrombocytopenic purpura [ORDO Disease]
- Thrombotic thrombocytopenic purpura, hereditary [OMIM Phenotype]
- Upshaw-Schulman syndrome (disorder) [SNOMED CT concept]
Related record
- purpura, thrombotic thrombocytopenic [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Thrombotic Thrombocytopenic Purpura [NCIt concept]
- Congenital thrombotic thrombocytopenic purpura [ORDO Disease]
- Thrombotic thrombocytopenic purpura, hereditary [OMIM Phenotype]
- Upshaw-Schulman syndrome (disorder) [SNOMED CT concept]