Human Phenotype Ontology 
Grandparent Node:
Abnormal eye morphology (HP:0012372)help
Grandparent Node:
Neoplasm by anatomical site (HP:0011793)help
Parent Node:
Neoplasm of the eye (HP:0100012)help
..Starting node
Orbital schwannoma (HP:0025604)help
Term ID: 25604
Name: Orbital schwannoma
Definition: A schwannoma (benign, usually encapsulated slow growing tumor composed of Schwann cells) located in the orbit.
Reference: HP:0025604
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandHamartoma of the eye (HP:0010568) help
..expandRetinal neoplasm (HP:0012777) help
..expandScleral schwannoma (HP:0100011) help
..expandUveal melanoma (HP:0007716) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025604HP:0025604Orbital schwannoma0 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 August 2021 release.