Abnormality of the kidney

Source:http://linkedlifedata.com/resource/phenotype/id/HP:0000077

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Statements in which the resource exists.
Subject	Predicate	Object	Context
phenotype:HP:0000077	rdf:type	skos:Concept	lld:phenotype
phenotype:HP:0000077	skos:definition	"An abnormality of the `kidney` (FMA:7203)." [HPO:curators]	lld:phenotype
phenotype:HP:0000077	skos:inScheme	lld:phenotype	lld:phenotype
phenotype:HP:0000077	skos:prefLabel	Abnormality of the kidney	lld:phenotype
phenotype:HP:0000077	skos:altLabel	Renal anomalies	lld:phenotype
phenotype:HP:0000077	skos:altLabel	Renal anomaly	lld:phenotype
phenotype:HP:0000077	skos:note	The kidney is a paired organ whose primary function is the production of urine.	lld:phenotype
phenotype:HP:0000077	skos:broader	phenotype:HP:0010935	lld:phenotype
phenotype:HP:0000077	skos:relatedSynonym	Kidney disease	lld:phenotype
phenotype:HP:0000107	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0000075	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0004742	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0100542	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0008678	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0100957	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0000091	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0000095	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0000123	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0100820	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0000105	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0011035	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0000110	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0000112	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0000121	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0000787	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0000790	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0000792	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0000799	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0001917	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0008776	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0001966	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0004712	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0004735	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0005575	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0010944	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0009726	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0008717	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0009741	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0010680	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0010685	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0011130	skos:broader	phenotype:HP:0000077	lld:phenotype
phenotype:HP:0100880	skos:broader	phenotype:HP:0000077	lld:phenotype