This HTML5 document contains 16 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

PrefixIRI
n7https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
rdfshttp://www.w3.org/2000/01/rdf-schema#
obohttp://www.geneontology.org/formats/oboInOwl#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DOID_0060880
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0060879
rdfs:label
renal hypomagnesemia 3
wdrs:describedby
n7:doid.owl
obo:id
DOID:0060880
obo:hasDbXref
ICD10CM:E83.4 ORDO:31043 OMIM:248250
obo:hasExactSynonym
isolated renal hypomagnesemia HOMG3 renal hypomagnesemia type 3 familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement primary hypomagnesemia due to defect in renal tubular transport of magnesium FHHNC without severe ocular involvement
obo:hasOBONamespace
disease_ontology
n2: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.