Human Phenotype Ontology 
Grandparent Node:
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Abnormality iris morphology (HP:0000525)help
Parent Node:
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Abnormal iris pigmentation (HP:0008034)help
..Starting node
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Iris pigment dispersion (HP:0012634)help
Term ID: 12634
Name: Iris pigment dispersion
Synonym:
Definition: Shedding of the pigment granules that normally adhere to the back of the iris into the aqueous humor.
Comments:
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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
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 December 15 2022 release.