hooft disease - CISMeF

Preferred Label : hooft disease;

MeSH note : Retarded physical development, erythematosquamous eruption, opaque leukonychia, mental retardation, and low serum lipids;

Details

Origin ID

C535329;

UMLS CUI

C0268479;

Currated CISMeF NLP mapping
- Hooft disease [OMIM Phenotype]
MeSH term(s) associated for indexing
- dyslipidemias [MeSH Descriptor]
- erythema [MeSH Descriptor]
- growth disorders [MeSH Descriptor]
- intellectual disability [MeSH Descriptor]
- nail diseases [MeSH Descriptor]
Record concept(s)
- Hooft disease [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hooft disease [OMIM Phenotype]
- Hooft's syndrome (disorder) [SNOMED CT concept]
- hooft's syndrome [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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