<http://purl.obolibrary.org/obo/DOID_0060880>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:E83.4"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060880>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"isolated renal hypomagnesemia"@en .
<http://purl.obolibrary.org/obo/DOID_0060880>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A hypomagnesemia characterized by autosomal recessive inheritance of excessive urinary Ca(2+) and Mg(2+) excretion that has material_basis_in homozygous or compound heterozygous mutation in the CLDN16 gene on chromosome 3q28."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060880>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"HOMG3"@en .
<http://purl.obolibrary.org/obo/DOID_0060880>	<http://www.w3.org/2000/01/rdf-schema#label>	"renal hypomagnesemia 3"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060880>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0060880"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060880>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"renal hypomagnesemia type 3"@en .
<http://purl.obolibrary.org/obo/DOID_0060880>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement"@en .
<http://purl.obolibrary.org/obo/DOID_0060880>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"primary hypomagnesemia due to defect in renal tubular transport of magnesium"@en .
<http://purl.obolibrary.org/obo/DOID_0060880>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:31043"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060880>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:248250"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060880>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0060879> .
<http://purl.obolibrary.org/obo/DOID_0060880>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
<http://purl.obolibrary.org/obo/DOID_0060880>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060880>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_0060880>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"FHHNC without severe ocular involvement"@en .