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 kidney (HP:0000077)

Grandparent Node:
Urinary tract neoplasm (HP:0010786)

Parent Node:
Renal neoplasm (HP:0009726)

..Starting node
..Renal pelvic carcinoma (HP:0006762)

Term ID:

6762

Name:

Renal pelvic carcinoma

Synonym:

Definition:

The presence of a carcinoma in the renal pelvis.

Comments:

Reference:

HP:0006762

Genes and Diseases:

Child Nodes:

Sister Nodes:

Embryonal renal neoplasm (HP:0011794)

Renal cell carcinoma (HP:0005584)

Renal cortical adenoma (HP:0006735)

Renal hamartoma (HP:0008696)

Renal oncocytoma (HP:0011798)

Renal sarcoma (HP:0008663)

Renal transitional cell carcinoma (HP:0030409)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006762	HP:0006762	Renal pelvic carcinoma	0	CL E G H

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.