Human Phenotype Ontology 
Grandparent Node:
Abnormality iris morphology (HP:0000525)help
Parent Node:
Abnormal iris pigmentation (HP:0008034)help
..Starting node
Iris pigment dispersion (HP:0012634)help
Term ID: 12634
Name: Iris pigment dispersion
Definition: Shedding of the pigment granules that normally adhere to the back of the iris into the aqueous humor.
Reference: HP:0012634
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAsymmetry of iris pigmentation (HP:0200064) help
..expandBlue irides (HP:0000635) help
..expandBrushfield spots (HP:0001088) help
..expandIris hypopigmentation (HP:0007730) help
..expandIris transillumination defect (HP:0012805) help
..expandStellate iris (HP:0012775) 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:0012634HP:0012634Iris pigment dispersion0 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 June 2019 release.