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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: Hypertension, Renal (D006977)
..Starting node ..Renoprival hypertension (C537760)
Child Nodes:
Sister Nodes:
..Hypertension, Renovascular (D006978)
..Hypertensive Nephropathy (C563161)
..Renoprival hypertension (C537760)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9674
Name:	Renoprival hypertension
Definition:
Alternative IDs:
ParentIDs:	MESH:D006977
TreeNumbers:	C12.777.419.331/C537760 \|C13.351.968.419.331/C537760 \|C14.907.489.631/C537760
Synonyms:
Slim Mappings:	Cardiovascular disease\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: C537760 MeSH: C537760 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants