About: Warburg micro syndrome

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

NT MGI.

Attributes	Values
type	Class
subClassOf	autosomal recessive disease syndrome nodeID://b50938520
label	Warburg micro syndrome
comment	NT MGI.
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0060237
created_by	emitraka
creation_date	2015-01-27T14:32:30Z
database_cross_reference	MESH:C536681 OMIM:PS600118 ORDO:2510 UMLS_CUI:C1838625
has_exact_synonym	WARBM (en) Warburg-Sjo-Fledelius syndrome (en) micro syndrome (en)
has_obo_namespace	disease_ontology
in_subset	DO_rare_slim
http://purl.obolib...g/obo/IAO_0000115	A syndrome characterized by severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis or hypoplasia of the corpus callosum and hypogenitalism.
is subClassOf of	Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50938521

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