Melanosis, universal

Preferred Label : Melanosis, universal;

Obsolete resource : true;

Moved to : 145250;

Inheritance : Autosomal dominant;

Prefixed ID : 155800;

Details

Origin ID

155800;

UMLS CUI

C1835039;

Currated CISMeF NLP mapping
- Familial progressive hyperpigmentation [ORDO Disease]
- Familial progressive hyperpigmentation (disorder) [SNOMED CT concept]
- Progressive hyperpigmentation [HPO term]
- hyperpigmentation, familial progressive [MeSH concept]
- hyperpigmentation, familial progressive [MeSH Supplementary Concept]
- melanosis, universal [MeSH concept]
- melanosis, universal [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- melanosis, universal [MeSH Supplementary Concept]
- melanosis, universal [MeSH concept]

Keyword's position in hierarchy(ies) :

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