Hemolytic disease of newborn, unspecified

Preferred Label : Hemolytic disease of newborn, unspecified;

Diag associé à un acte (%) : 50.9;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

P559;

UMLS CUI

C0014761;

Orphanet concepts
- Hemolytic disease due to fetomaternal alloimmunization [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Erythroblastosis fetalis [MedDRA LLT]
- Erythroblastosis foetalis [MedDRA Preferred Term]
- Haemolytic disease of foetus or newborn, due to isoimmunisation [MedDRA LLT]
- Hemolytic Disease of the Newborn [NCIt concept]
- Hemolytic disease of fetus OR newborn due to isoimmunization (disorder) [SNOMED CT concept]
- Hemolytic disease of fetus or newborn due to other and unspecified isoimmunization [ICD-9 code]
- Hemolytic disease of fetus or newborn, due to isoimmunization [MedDRA LLT]
- Hemolytic disease of fetus or newborn, due to isoimmunization [ICD-9 code]
- erythroblastosis, fetal [MeSH Descriptor]
- erythroblastosis, fetal [MeSH concept]
- fetal erythroblastosis [DO Concept]
- hemolytic disease of fetus or newborn due to isoimmunization, nos [SNOMED Notion]
- hemolytic disease of fetus or newborn, nos [SNOMED Notion]
- newborn hemolytic disorder [Disease (Nov.)]
Validated automatic mappings to NTBT
- Hemolytic Disease of the Newborn [NCIt concept]

Keyword's position in hierarchy(ies) :

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