Nephrogenic Diabetes Insipidus, Type II

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Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	umls-semnetwork:T047, skos:Concept
calbc:hasCorrelation	calbc-group:CONC, calbc-group:DISO, calbc-group:PHEN
skos:definition	MSH: Congenital nephrogenic diabetes insipidus caused by mutations of the aquaporin-2 water channel gene (AOP2) on chromosome 12q13.
skos:inScheme	lld:umls
skos-xl:prefLabel	umls-label:A8417417
skos-xl:altLabel	umls-label:A11992857, umls-label:A8409479, umls-label:A20907270, umls-label:A11992856