Human Phenotype Ontology

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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

Grandparent Node:
Abnormality of the genitourinary system (HP:0000119)

Parent Node:
Abnormality of the urinary system (HP:0000079)

..Starting node
..Abnormality of the upper urinary tract (HP:0010935)

Term ID:	10935
Name:	Abnormality of the upper urinary tract
Synonym:	Abnormality of the upper urinary tract
Definition:	An abnormality of the upper urinary tract.
Comments:
Reference:	HP:0010935
Genes and Diseases:	There are 577 terms for your input, too many to show detail here. Please try its child terms.
Child Nodes:
........Abnormality of the ureter (HP:0000069) ................... HP:0000070 Ureterocele ................... HP:0000072 Hydroureter ................... HP:0000073 Ureteral duplication ................... HP:0000076 Vesicoureteral reflux ................... HP:0005999 Ureteral atresia ................... HP:0006000 Ureteral obstruction ................... HP:0008631 Ureteral dysgenesis ................... HP:0008676 Congenital megaureter ................... HP:0012300 Ureteral agenesis ................... HP:0100516 Neoplasm of the ureter
........Abnormality of the kidney (HP:0000077) ................... HP:0009726 Renal neoplasm ................... HP:0012210 Abnormal renal morphology ................... HP:0012211 Abnormal renal physiology
Sister Nodes:
..Abnormality of the lower urinary tract (HP:0010936)
..Abnormality of the urinary system physiology (HP:0011277)
..Urinary tract atresia (HP:0000809)
Genes (0) : Diseases (0) :
Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.