elliptocytosis, hereditary

Preferred Label : elliptocytosis, hereditary;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0007240;

UMLS CUI

C0013902;

Automatic exact mappings (from CISMeF team)
- Hereditary elliptocytosis [PASCAL descriptor]
Currated CISMeF NLP mapping
- Congenital elliptocytosis (disorder) [SNOMED CT concept]
- Elliptocytosis [HPO term]
- Elliptocytosis hereditary [MedDRA Preferred Term]
- Hereditary Elliptocytosis [NCIt concept]
- Hereditary elliptocytosis [ICD-10 Sub-category]
- Hereditary elliptocytosis [ICD-11 Subcategory]
- Hereditary elliptocytosis [ICD-10 Sub-category (who)]
- Hereditary elliptocytosis [ICD-9 code]
- Hereditary elliptocytosis [ORDO Disease]
- Hereditary elliptocytosis [MedDRA LLT]
- Hereditary elliptocytosis (disorder) [SNOMED CT concept]
- hereditary elliptocytosis [DO Concept]
- hereditary elliptocytosis, nos [SNOMED Notion]
Related record
- elliptocytosis, hereditary [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital elliptocytosis (disorder) [SNOMED CT concept]
- Elliptocytosis hereditary [MedDRA Preferred Term]
- Hereditary Elliptocytosis [NCIt concept]
- Hereditary elliptocytosis [ICD-9 code]
- Hereditary elliptocytosis [ORDO Disease]
- Hereditary elliptocytosis [ICD-10 Sub-category]
- Hereditary elliptocytosis [ICD-10 Sub-category (who)]
- Hereditary elliptocytosis [ICD-11 Subcategory]
- Hereditary elliptocytosis [MedDRA LLT]
- Hereditary elliptocytosis (disorder) [SNOMED CT concept]
- hereditary elliptocytosis [DO Concept]
- hereditary elliptocytosis, nos [SNOMED Notion]