Eliptocitosis Hereditaria

Preferred Label : Eliptocitosis Hereditaria;

DeCS synonym : Ovalocitosis Hereditaria;

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

Details

Origin ID

D004612;

UMLS CUI

C0013902;

Currated CISMeF NLP mapping
- ELIPTOCITOSIS HEREDITARIA [ICD-9 code]
- Eliptocitosis hereditaria [MedDRA Preferred Term]
- Eliptocitosis hereditaria [ORDO Disease]
- Eliptocitosis hereditaria [MedDRA LLT]
- eliptocitosis congénita (trastorno) [Concepto SNOMED CT]
- eliptocitosis hereditaria (trastorno) [Concepto SNOMED CT]
False automatic mappings
- eliptocitosis congénita (trastorno) [Concepto SNOMED CT]
ORDO relation(s)
- Eliptocitosis hereditaria [ORDO Disease]
See also
- Anemia Sideroblástica [MeSH Descriptor]
UMLS correspondences (same concept)
- ELIPTOCITOSIS HEREDITARIA [ICD-9 code]
- Eliptocitosis hereditaria [ORDO Disease]
- Eliptocitosis hereditaria [MedDRA Preferred Term]
- Eliptocitosis hereditaria [MedDRA LLT]
- eliptocitosis congénita (trastorno) [Concepto SNOMED CT]
- eliptocitosis hereditaria (trastorno) [Concepto SNOMED CT]

Keyword's position in hierarchy(ies) :

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