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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Asymmetry of iris pigmentation (HP:0200064)help
Term ID: 200064
Name: Asymmetry of iris pigmentation
Synonym:
Definition: Asymmetry between the two irides or asymmetry between different parts of one iris.
Comments:
Reference: HP:0200064
Genes and Diseases:
 
       Child Nodes:
........expandHeterochromia iridis (HP:0001100) help
................... HP:0007818 Central heterochromia
................... HP:0009781 Lester's sign

 Sister Nodes: 
..expandBlue irides (HP:0000635) help
..expandBrushfield spots (HP:0001088) help
..expandIris hypopigmentation (HP:0007730) help
..expandIris pigment dispersion (HP:0012634) 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:0200064HP:0200064Asymmetry of iris pigmentation0 CL E G H
HP:0200064HP:0200064Asymmetry of iris pigmentation1 CL E G H
HP:0200064HP:0200064Asymmetry of iris pigmentation2 CL E G H


Genes (19) :ACTB ACTG1 AKT1 CHN1 COL25A1 EDN3 EDNRB ELP1 GNAQ KIT KITLG LMX1B MAFB MITF PAX3 PNPLA6 PTEN SNAI2 SOX10

Diseases (22) :2995 613265 895 277580 1764 3205 2884 172800 193510 894 148820 193500 2969 608890 163746 609136 611584 613266 744 233 161200 275400
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.