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Namespace Prefixes

PrefixIRI
n6https://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_0110142
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_445
rdfs:label
Bartter disease type 1
wdrs:describedby
n6:doid.owl
obo:id
DOID:0110142
obo:hasDbXref
OMIM:601678 ICD10CM:E26.8
obo:hasExactSynonym
BARTS1 Bartter syndrome type 1 antenatal hypokalemic alkalosis with hypercalciuria 1 antenatal hyperprostaglandin E syndrome 1 Bartter syndrome type 1
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the sodium-potassium-chloride cotransporter-2 gene (SLC12A1) on chromosome 15q21.