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Human Disease Ontology
Last uploaded:
November 27, 2024
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| Preferred Name | dyschromatosis universalis hereditaria | |
| Synonyms |
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| Definitions |
A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution. NT MGI. |
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| ID |
http://purl.obolibrary.org/obo/DOID_0060304 |
|
| comment |
NT MGI.
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|
| created_by |
emitraka
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| creation_date |
2015-02-09T16:53:42Z
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| database_cross_reference |
MESH:C535730 NCI:C173131 UMLS_CUI:C2930995 GARD:1996 MIM:127500 MIM:612715 MIM:615402 ORDO:241
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|
| definition |
A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution.
|
|
| has_obo_namespace |
disease_ontology
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|
| id |
DOID:0060304
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| in_subset | ||
| label |
dyschromatosis universalis hereditaria
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| notation |
DOID:0060304
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| prefLabel |
dyschromatosis universalis hereditaria
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| subClassOf |
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