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About:
dyschromatosis universalis hereditaria
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An Entity of Type :
owl:Class
, within Data Space :
linkeddata.uriburner.com:28898
associated with source
document(s)
New Facet based on Instances of this Class
NT MGI.
Attributes
Values
type
Class
subClassOf
pigmentation disease
label
dyschromatosis universalis hereditaria
comment
NT MGI.
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0060304
created_by
emitraka
creation_date
2015-02-09T16:53:42Z
database_cross_reference
GARD:1996
MESH:C535730
NCI:C173131
OMIM:127500
OMIM:612715
OMIM:615402
ORDO:241
UMLS_CUI:C2930995
has_obo_namespace
disease_ontology
in_subset
DO_rare_slim
http://purl.obolib...g/obo/IAO_0000115
A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution.
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50938617
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