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Namespace Prefixes

Prefix	IRI
n5	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Statements

Subject Item

n2:DOID_0060885

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_0060879

rdfs:label

renal hypomagnesemia 2

wdrs:describedby

n5:doid.owl

obo:id

DOID:0060885

obo:hasDbXref

ORDO:34528 OMIM:154020 GARD:3350 ICD10CM:E83.4

obo:hasExactSynonym

HOMG2 autosomal dominant primary hypomagnesemia with hypocalciuria

obo:hasOBONamespace

disease_ontology

n2:IAO_0000115

A hypomagnesemia characterized by autosomal dominant inheritance of hypomagnesemia due to renal magnesium loss that has material_basis_in heterozygous mutation in the FXYD2 gene on chromosome 11q23.