dyschromatosis symmetrica hereditaria 1

Preferred Label : dyschromatosis symmetrica hereditaria 1;

MeSH synonym : symmetric dyschromatosis of the extremities; reticulate acropigmentation of dohi; dyschromatosis symmetrica hereditaria; familial reticulate acropigmentation of dohi;

Details

Origin ID

C535729;

UMLS CUI

C0406775;

Automatic exact mappings (from CISMeF team)
- Dohi acropigmentation [PASCAL descriptor]
Currated CISMeF NLP mapping
- Dyschromatosis Symmetrica Hereditaria [NCIt concept]
- Dyschromatosis symmetrica hereditaria [OMIM Phenotype]
- Dyschromatosis symmetrica hereditaria [ORDO Disease]
- Hereditary symmetrical dyschromatosis [ICD-11 More detail]
- Symmetrical dyschromatosis of extremities (disorder) [SNOMED CT concept]
- dyschromatosis symmetrica hereditaria [DO Concept]
- dyschromatosis symmetrica hereditaria [Disease (Nov.)]
DO Cross reference
- dyschromatosis symmetrica hereditaria [DO Concept]
MeSH term(s) associated for indexing
- pigmentation disorders [MeSH Descriptor]
ORDO relation(s)
- Dyschromatosis symmetrica hereditaria [ORDO Disease]
Record concept(s)
- Dyschromatosis symmetrica hereditaria 1 [MeSH concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Dyschromatosis Symmetrica Hereditaria [NCIt concept]
- Dyschromatosis symmetrica hereditaria [ORDO Disease]
- Dyschromatosis symmetrica hereditaria [OMIM Phenotype]
- Hereditary symmetrical dyschromatosis [ICD-11 More detail]
- Symmetrical dyschromatosis of extremities (disorder) [SNOMED CT concept]
- dyschromatosis symmetrica hereditaria [DO Concept]
- dyschromatosis symmetrica hereditaria [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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