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:
Neoplasm by histology (HP:0011792)

Parent Node:
Renal neoplasm (HP:0009726)

Parent Node:
Sarcoma (HP:0100242)

..Starting node
..Renal sarcoma (HP:0008663)

Term ID:

8663

Name:

Renal sarcoma

Synonym:

Definition:

A sarcoma of the kidney.

Comments:

Reference:

HP:0008663

Genes and Diseases:

Child Nodes:

Sister Nodes:

Chondrosarcoma (HP:0006765)

Ewing sarcoma (HP:0012254)

Osteosarcoma (HP:0002669)

Soft tissue sarcoma (HP:0030448)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008663	HP:0008663	Renal sarcoma	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.