Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the lens (HP:0000517)help
Parent Node:
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Cataract (HP:0000518)help
..Starting node
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Capsular cataract (HP:0100017)help
Term ID: 100017
Name: Capsular cataract
Synonym:
Definition: A cataract that affects the capsule of the lens.
Comments:
Reference: HP:0100017
Genes and Diseases:
 
       Child Nodes:
........expandPosterior capsular cataract (HP:0100020) help

 Sister Nodes: 
..expandAge-related cataract (HP:0011141) help
..expandChristmas tree cataract (HP:0025571) help
..expandDevelopmental cataract (HP:0000519) help
..expandJuvenile cataract (HP:0001118) help
..expandMembranous cataract (HP:0010922) help
..expandobsolete Total cataract (HP:0010700) help
..expandPolar cataract (HP:0010696) help
..expandPresenile cataracts (HP:0007819) help
..expandProgressive cataract (HP:0007834) help
..expandSubcapsular cataract (HP:0000523) help
..expandZonular cataract (HP:0010920) 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:0100017HP:0100017Capsular cataract0 CL E G H
HP:0100017HP:0100017Capsular cataract1 CL E G H


Genes (1) :CRYAB

Diseases (1) :399058
 

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