Esferocitosis Hereditaria - CISMeF

CISMeF

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Esferocitosis HereditariaDescripteur MeSH

Preferred Label : Esferocitosis Hereditaria;

Wikipedia link : https://es.wikipedia.org/wiki/Esferocitosis hereditaria;

Details

Origin ID

D013103;

UMLS CUI

C0037889;

Manual NTBT mappings (CISMeF)
- Anemia hemolítica constitucional rara [ORDO Disease]
- Anemia hemolítica constitucional rara por una anomalía de la membrana eritrocitaria [ORDO Disease]
ORDO relation(s)
- Esferocitosis hereditaria [ORDO Disease]
See also
- Anemia Sideroblástica [MeSH Descriptor]
- Proteína 1 de Intercambio de Anión de Eritrocito [MeSH Descriptor]
UMLS correspondences (same concept)
- Anemia esferocítica [MedDRA LLT]
- Anemia esferocítica [MedDRA Preferred Term]
- Anemia esferocítica [MedDRA LLT]
- Anemia esferocítica [MedDRA LLT]
- ESFEROCITOSIS HEREDITARIA [ICD-9 code]
- Esferocitosis hereditaria [ORDO Disease]
- Esferocitosis hereditaria [MedDRA Preferred Term]
- Síndrome de Minkowski-Chauffard [MedDRA LLT]
- anemia esferocitica [WHO-ART Preferred Term]
- esferocitosis hereditaria (trastorno) [Concepto SNOMED CT]

Keyword's position in hierarchy(ies) :

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20/06/2025

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