Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal anterior eye segment morphology (HP:0004328)help
Grandparent Node:
expand
Abnormal uvea morphology (HP:0000553)help
Parent Node:
expand
Abnormality iris morphology (HP:0000525)help
..Starting node
..expand
Iridodonesis (HP:0100693)help
Term ID: 100693
Name: Iridodonesis
Synonym:
Definition: Tremulousness of the iris on movement of the eye, occurring in subluxation of the lens.
Comments:
Reference: HP:0100693
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal iris pigmentation (HP:0008034) help
..expandAbnormal iris vasculature (HP:0007905) help
..expandAbnormal pupil morphology (HP:0000615) help
..expandAplasia/Hypoplasia of the iris (HP:0008053) help
..expandIris atrophy (HP:0001089) help
..expandIris coloboma (HP:0000612) help
..expandIris cyst (HP:0011523) help
..expandIris flocculi (HP:0500007) help
..expandIris melanoma (HP:0011524) help
..expandIris nevus (HP:0011525) help
..expandIritis (HP:0001101) help
..expandLisch nodules (HP:0009737) help
..expandUveal ectropion (HP:0025358) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0100693HP:0100693Iridodonesis0ADAMTS17 CL E G H170691613195Weill-Marchesani-like syndrome613195C2750787OMIM1848217109607511
HP:0100693HP:0100693Iridodonesis0CHRDL1 CL E G H91851309300Megalocornea309300C0344530OMIM12118229861300350
HP:0100693HP:0100693Iridodonesis0CPAMD8 CL E G H27151617319Anterior segment dysgenesis 8617319C4310622OMIM165823228608841
HP:0100693HP:0100693Iridodonesis0FBN1 CL E G H2200284979ORPHA1272142843603134797
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100693HP:0100693Iridodonesis0LTBP2 CL E G H4053251750Microspherophakia251750C1562061OMIM0292996715602091


Genes (5) :ADAMTS17 CHRDL1 CPAMD8 FBN1 LTBP2

Diseases (5) :613195 309300 617319 284979 251750
 

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