Human Phenotype Ontology 
Grandparent Node:
Melanoma (HP:0002861)help
Grandparent Node:
Neoplasm of the eye (HP:0100012)help
Parent Node:
Abnormality iris morphology (HP:0000525)help
Parent Node:
Uveal melanoma (HP:0007716)help
..Starting node
Iris melanoma (HP:0011524)help
Term ID: 11524
Name: Iris melanoma
Definition: Malignant tumor of melanocytes affecting the iris.
Reference: HP:0011524
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandChoroidal melanoma (HP:0012054) help
..expandCiliary body melanoma (HP:0012055) 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:0011524HP:0011524Iris melanoma0BAP1 CL E G H8314950ORPHA:39044Uveal melanomaHP:0040282 - Frequent184
HP:0011524HP:0011524Iris melanoma0CYSLTR2 CL E G H5710518274ORPHA:39044Uveal melanomaHP:0040282 - Frequent1
HP:0011524HP:0011524Iris melanoma0GNA11 CL E G H27674379ORPHA:39044Uveal melanomaHP:0040282 - Frequent16
HP:0011524HP:0011524Iris melanoma0GNAQ CL E G H27764390ORPHA:39044Uveal melanomaHP:0040282 - Frequent7
HP:0011524HP:0011524Iris melanoma0SF3B1 CL E G H2345110768ORPHA:39044Uveal melanomaHP:0040282 - Frequent19

Genes (5) :BAP1 CYSLTR2 GNA11 GNAQ SF3B1

Diseases (1) :ORPHA:39044

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.