Lentiginosis, centrofacial neurodysraphic

Preferred Label : Lentiginosis, centrofacial neurodysraphic;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Lentiginosis, touraine type;

Inheritance : Autosomal dominant;

Prefixed ID : 151000;

Details

Origin ID

151000;

UMLS CUI

C1835484;

Currated CISMeF NLP mapping
- lentiginosis, centrofacial neurodysraphic [MeSH concept]
- lentiginosis, centrofacial neurodysraphic [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the skin [HPO term]
- Autosomal dominant inheritance [HPO term]
- Intellectual disability [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- lentiginosis, centrofacial neurodysraphic [MeSH Supplementary Concept]
- lentiginosis, centrofacial neurodysraphic [MeSH concept]

Keyword's position in hierarchy(ies) :

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