About: intestinal hypomagnesemia 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	primary hypomagnesemia
label	intestinal hypomagnesemia 1
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0060883
database_cross_reference	ICD10CM:E83.4 OMIM:602014 ORDO:30924
has_exact_synonym	HOMG1 (en) hypomagnesemia caused by selective magnesium malabsorption (en) hypomagnesemia intestinal type 1 (en) hypomagnesemic tetany (en) primary hypomagnesemia with secondary hypocalcemia (en) intestinal hypomagnesemia with secondary hypocalcemia (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A hypomagnesemia characterized by very low serum magnesium levels due to defects in intestinal absorbtion and kidney excretion and secondary hypocalcemia that has material_basis_in homozygous or compound heterozygous mutations in the TRPM6 gene on chromosome 9q21.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50939551

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