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Prefix	IRI
n7	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#

Subject Item: n2:DOID_0060781
rdf:type: owl:Class
rdfs:subClassOf: n2:DOID_0050737 n2:DOID_0080015 n2:DOID_0050129 _:vb50939381 _:vb50939382 _:vb50939383
rdfs:label: congenital secretory sodium diarrhea 3
wdrs:describedby: n7:doid.owl
obo:id: DOID:0060781
obo:hasDbXref: ICD10CM:P78.3 OMIM:270420 ORDO:103908
obo:hasExactSynonym: congenital secretory sodium diarrhoea 3 congenital secretory sodium diarrhea 3 syndromic congenital secretory sodium diarrhea 3 with or without other congenital anomalies congenital secretory sodium diarrhoea 3 with or without other congenital anomalies congenital secretory sodium diarrhoea 3 syndromic
obo:hasOBONamespace: disease_ontology
n2:IAO_0000115: A secretory diarrhea that has_material_basis_in homozygous or compound heterozygous mutation in the SPINT2 gene on chromosome 19q13.