About: Feingold syndrome

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

Attributes	Values
type	Class
subClassOf	autosomal dominant disease syndrome nodeID://b50938887
label	Feingold syndrome
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0060464
created_by	elvira
creation_date	2015-11-04T16:11:58Z
database_cross_reference	GARD:8407 ICD10CM:Q87.8 MESH:C537734 OMIM:164280 OMIM:614326 ORDO:1305
has_exact_synonym	microcephaly-oculo-digito-esophageal-duodenal syndrome (en) microcephaly-digital anomalies-normal intelligence syndrome (en) FGLDS (en) MODED syndrome (en) ODED syndrome (en) oculo-digito-esophageal-duodenal syndrome (en) digital anomalies with short palpebral fissures and atresia of esophagus or duodenum (en)
has_obo_namespace	disease_ontology
in_subset	DO_rare_slim
http://purl.obolib...g/obo/IAO_0000115	A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50938888

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