Graying of hair, precocious

Preferred Label : Graying of hair, precocious;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : White hair, premature;

Inheritance : Autosomal dominant form;

Prefixed ID : %139100;

Details

Origin ID

139100;

UMLS CUI

C1841809;

Currated CISMeF NLP mapping
- Premature graying of body hair [HPO term]
- graying of hair, precocious [MeSH concept]
- graying of hair, precocious [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Premature graying of hair [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- graying of hair, precocious [MeSH Supplementary Concept]
- graying of hair, precocious [MeSH concept]

Keyword's position in hierarchy(ies) :

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