Wolman disease with hypolipoproteinemia and acanthocytosis

Preferred Label : Wolman disease with hypolipoproteinemia and acanthocytosis;

Obsolete resource : true;

Moved to : 278000;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 278100;

Détails

Origin ID

278100;

UMLS CUI

C1848436;

Currated CISMeF NLP mapping
- wolman disease with hypolipoproteinemia and acanthocytosis [MeSH concept]
- wolman disease with hypolipoproteinemia and acanthocytosis [MeSH Supplementary Concept]
HPO term(s)
- Growth failure [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- wolman disease with hypolipoproteinemia and acanthocytosis [MeSH Supplementary Concept]
- wolman disease with hypolipoproteinemia and acanthocytosis [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

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