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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Presenile cataracts (HP:0007819)help
Term ID: 7819
Name: Presenile cataracts
Synonym: Presenile cataract
Definition: Presenile cataract is a kind of cataract that occurs in early adulthood, that is, at an age that is younger than usual.
Comments:
Reference: HP:0007819
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAge-related cataract (HP:0011141) help
..expandCapsular cataract (HP:0100017) 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
..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:
HP:0007819HP:0007819Presenile cataracts0MTAP CL E G H4507112250Diaphyseal medullary stenosis with malignant fibrous histiocytoma112250C1862177OMIM122087413156540
HP:0007819HP:0007819Presenile cataracts0PAX6 CL E G H5080136520Foveal hypoplasia and presenile cataract syndrome136520C3805604OMIM15714968620607108
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (2) :MTAP PAX6

Diseases (2) :112250 136520
 

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