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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: Heart Failure (D006333)
Parent Node: Renal Insufficiency (D051437)
..Starting node ..Cardio-Renal Syndrome (D059347)
Child Nodes:
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:	1765
Name:	Cardio-Renal Syndrome
Definition:	Condition where a primary dysfunction of either heart or kidney results in failure of the other organ (e.g., HEART FAILURE with worsening RENAL INSUFFICIENCY).
Alternative IDs:
ParentIDs:	MESH:D006333\|MESH:D051437
TreeNumbers:	C12.777.419.780.400 \|C13.351.968.419.780.400 \|C14.280.434.156
Synonyms:	Cardiorenal Syndrome \|Cardio Renal Syndrome \|Cardiorenal Syndromes \|Cardio-Renal Syndromes \|Renocardiac Syndrome \|Reno Cardiac Syndrome \|Reno-Cardiac Syndrome \|Renocardiac Syndromes \|Reno-Cardiac Syndromes \|Syndrome, Cardiorenal \|Syndrome, Cardio-Renal \|Syndrome, R
Slim Mappings:	Cardiovascular disease\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: D059347 MeSH: D059347 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants