About: autosomal dominant hypocalcemia

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

Attributes	Values
type	Class
subClassOf	autosomal dominant disease metal metabolism disorder nodeID://b50942271
label	autosomal dominant hypocalcemia
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0090109
database_cross_reference	GARD:2877 ICD10CM:E20.8 OMIM:PS601198 ORDO:428
has_exact_synonym	HYPOC (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A metal metabolism disorder characterized by autosomal dominant inheritance of variable degrees of hypocalcemia with normal to low levels of parathyroid hormone.
is subClassOf of	autosomal dominant hypocalcemia 1 autosomal dominant hypocalcemia 2
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50942272

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