rh deficiency syndrome

Preferred Label : rh deficiency syndrome;

Origin ID

DC-15580;

UMLS CUI

C0272052;

Automatic exact mappings (from CISMeF team)
- Rh-null, regulator type [OMIM Phenotype]
Currated CISMeF NLP mapping
- Rh deficiency syndrome [DO Concept]
- Rh deficiency syndrome [ICD-11 More detail]
- Rh deficiency syndrome [ORDO Disease]
- Rh deficiency syndrome (disorder) [SNOMED CT concept]
- rh deficiency syndrome [MeSH concept]
- rh deficiency syndrome [MeSH Supplementary Concept]
Manual NTBT mappings (CISMeF)
- Rare constitutional hemolytic anemia [ORDO Disease]
Metaterm(s)
- hematology [CISMeF Metaterm]
SNOMED CT concept
- Rh deficiency syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Rh deficiency syndrome [ORDO Disease]
- Rh deficiency syndrome [DO Concept]
- Rh deficiency syndrome [ICD-11 More detail]
- Rh deficiency syndrome (disorder) [SNOMED CT concept]
- rh deficiency syndrome [MeSH Supplementary Concept]
- rh deficiency syndrome [MeSH concept]