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Experimental Factor Ontology
Preferred Name | dyschromatosis universalis hereditaria | |
Synonyms |
DUH dyschromatosis universalis |
|
Definitions |
A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution. |
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ID |
http://purl.obolibrary.org/obo/MONDO_0000736 |
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database_cross_reference |
SCTID:239082002 DOID:0060304 MESH:C535730 NCIT:C173131 MEDGEN:419691 OMIMPS:127500 Orphanet:241 UMLS:C2930995 GARD:1996
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|
definition |
A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution.
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exactMatch |
https://omim.org/phenotypicSeries/PS127500 http://linkedlifedata.com/resource/umls/id/C2930995 http://purl.obolibrary.org/obo/DOID_0060304 http://purl.obolibrary.org/obo/NCIT_C173131 http://identifiers.org/mesh/C535730 http://purl.obolibrary.org/obo/Orphanet_241 |
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has_exact_synonym |
dyschromatosis universalis
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has_related_synonym |
DUH
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id |
MONDO:0000736
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in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-base#rare http://purl.obolibrary.org/obo/mondo/mondo-base#otar http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare http://purl.obolibrary.org/obo/mondo/mondo-base#orphanet_rare http://purl.obolibrary.org/obo/mondo/mondo-base#nord_rare http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_disorder |
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label |
dyschromatosis universalis hereditaria
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notation |
MONDO:0000736
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preferred label |
dyschromatosis universalis hereditaria
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prefLabel |
dyschromatosis universalis hereditaria
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see also |
https://rarediseases.info.nih.gov/diseases/1996/dyschromatosis-universalis-hereditaria |
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subClassOf |
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