Human Phenotype Ontology 
Grandparent Node:
expandNeoplasm of striated muscle (HP:0009728)help
Grandparent Node:
expandSoft tissue sarcoma (HP:0030448)help
Parent Node:
expandRhabdomyosarcoma (HP:0002859)help
..Starting node
..expandOrbital rhabdomyosarcoma (HP:0500092)help
Term ID: 500092
Name: Orbital rhabdomyosarcoma
Synonym:
Definition: A mesenchymal tumour that is considered to be the commonest primary orbital malignancy in children. Histologically, it may be differentiated into embryonal, alveolar, and pleomorphic types. It is usually intraconal or within the superior orbit.
Comments:
Reference: HP:0500092
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAlveolar rhabdomyosarcoma (HP:0006779) help
..expandEmbryonal rhabdomyosarcoma (HP:0006743) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0500092HP:0500092Orbital rhabdomyosarcoma0 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.