About: glucocorticoid deficiency 1

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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 recessive disease familial glucocorticoid deficiency nodeID://b50941345
label	glucocorticoid deficiency 1 (en)
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0080621
database_cross_reference	OMIM:202200
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A familial glucocorticoid deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding melanocortin-2 receptor, which is also referred to as adrenocorticotropin receptor, on chromosome 18p11.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50941346

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