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Preferred Name

Dyschromatosis Universalis Hereditaria
ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C173131
code

C173131
Concept_In_Subset

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C192842

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C165258
Contributing_Source

Cellosaurus
DEFINITION

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

Dyschromatosis Universalis Hereditaria
label

Dyschromatosis Universalis Hereditaria
Preferred_Name

Dyschromatosis Universalis Hereditaria
prefixIRI

Thesaurus:C173131
prefLabel

Dyschromatosis Universalis Hereditaria
Semantic_Type

Disease or Syndrome
UMLS_CUI

C2930995
subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C28193
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MESH/C535730 Medical Subject Headings / 医学主题词表 LOOM
http://purl.obolibrary.org/obo/DOID_0060304 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0000736 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0000736 Experimental Factor Ontology / 实验性因素本体 LOOM
http://www.orpha.net/ORDO/Orphanet_241 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM