wolman disease with hypolipoproteinemia and acanthocytosis

Preferred Label : wolman disease with hypolipoproteinemia and acanthocytosis;

Origin ID

C564736;

UMLS CUI

C0043208;

Currated CISMeF NLP mapping
- Wolman disease with hypolipoproteinemia and acanthocytosis [OMIM Phenotype]
MeSH term(s) associated for indexing
- abetalipoproteinemia [MeSH Descriptor]
- hypolipoproteinemias [MeSH Descriptor]
- wolman disease [MeSH Descriptor]
Record concept(s)
- wolman disease with hypolipoproteinemia and acanthocytosis [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Lysosomal acid lipase deficiency [OMIM Phenotype]
- Wolman Disease [NCIt concept]
- Wolman disease [ICD-11 More detail]
- Wolman disease [DO Concept]
- Wolman disease [Disease (Nov.)]
- Wolman disease [ORDO Disease]
- Wolman disease with hypolipoproteinemia and acanthocytosis [OMIM Phenotype]
- Wolman's disease [MedDRA LLT]
- Wolman's disease (disorder) [SNOMED CT concept]
- acid lipase deficiency, nos [SNOMED Notion]
- wolman's disease [MedDRA Preferred Term]
- wolman's disease [SNOMED Notion]