Dyschromatosis Universalis Hereditaria

Preferred Label : Dyschromatosis Universalis Hereditaria;

NCIt definition : A genetically heterogenous condition, usually inherited in an autosomal dominant fashion, characterized by hypopigmented and hyperpigmented macules involving the entire body surface.;

Details

Origin ID

C173131;

UMLS CUI

C2930995;

Currated CISMeF NLP mapping
- Dyschromatosis universalis hereditaria [MeSH concept]
- Dyschromatosis universalis hereditaria [PASCAL descriptor]
- Dyschromatosis universalis hereditaria [ORDO Disease]
- Dyschromatosis universalis hereditaria [OMIM phenotypic series]
- Hereditary universal dyschromatosis [ICD-11 More detail]
- dyschromatosis universalis hereditaria [MeSH Supplementary Concept]
- dyschromatosis universalis hereditaria [DO Concept]
DO Cross reference
- dyschromatosis universalis hereditaria [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dyschromatosis universalis hereditaria [MeSH concept]
- dyschromatosis universalis hereditaria [MeSH Supplementary Concept]
- dyschromatosis universalis hereditaria [DO Concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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