Hyperpigmentation of fuldauer and kuijpers

Preferred Label : Hyperpigmentation of fuldauer and kuijpers;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 145200;

Details

Origin ID

145200;

UMLS CUI

C1840393;

Currated CISMeF NLP mapping
- hyperpigmentation of fuldauer and kuijpers [MeSH concept]
- hyperpigmentation of fuldauer and kuijpers [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hyperpigmentation of the skin [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- hyperpigmentation of fuldauer and kuijpers [MeSH Supplementary Concept]
- hyperpigmentation of fuldauer and kuijpers [MeSH concept]

Keyword's position in hierarchy(ies) :

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