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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Renal Insufficiency (D051437)
..Starting node ..Renal Insufficiency, Chronic (D051436)
Child Nodes:
........Kidney Failure, Chronic (D007676) 3
Sister Nodes:
..Acute Kidney Injury (D058186) 2
..Arthrogryposis renal dysfunction cholestasis syndrome (C535382)
..Cardio-Renal Syndrome (D059347)
..EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE (OMIM:254900)
..Hyperuricemic Nephropathy, Familial Juvenile 2 (C567760)
..Lutz Richner Landolt syndrome (C537726)
..Nephrolithiasis, X-Linked Recessive, with Renal Failure (C562901)
..Papillorenal syndrome (C537168)
..Renal Insufficiency, Chronic (D051436) 4
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9659
Name:	Renal Insufficiency, Chronic
Definition:	Conditions in which the KIDNEYS perform below the normal level for more than three months. Chronic kidney insufficiency is classified by five stages according to the decline in GLOMERULAR FILTRATION RATE and the degree of kidney damage (as measured by the level of PROTEINURIA). The most severe form is the end-stage renal disease (CHRONIC KIDNEY FAILURE). (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002)
Alternative IDs:
ParentIDs:	MESH:D051437
TreeNumbers:	C12.777.419.780.750 \|C13.351.968.419.780.750
Synonyms:	Chronic Kidney Disease \|Chronic Kidney Diseases \|Chronic Kidney Insufficiencies \|Chronic Kidney Insufficiency \|Chronic Renal Disease \|Chronic Renal Diseases \|Chronic Renal Insufficiencies \|Chronic Renal Insufficiency \|Disease, Chronic Kidney \|Disease, Chronic Ren
Slim Mappings:	Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: D051436 MeSH: D051436 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants