Human Phenotype Ontology 
Grandparent Node:
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Cataract (HP:0000518)help
Parent Node:
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Subcapsular cataract (HP:0000523)help
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Posterior subcapsular cataract (HP:0007787)help
Term ID: 7787
Name: Posterior subcapsular cataract
Synonym: Posterior subcapsular cataracts; Posterior subcapsular opacities of the lens
Definition: A type of cataract affecting the posterior pole of lens immediately adjacent to ('beneath') the Lens capsule.
Comments:
Reference: HP:0007787
Genes and Diseases:
 
       Child Nodes:
........expandIridescent posterior subcapsular cataract (HP:0007889) help
........expandJuvenile posterior subcapsular lenticular opacities (HP:0007935) help

 Sister Nodes: 
..expandAnterior subcapsular cataract (HP:0010923) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007787HP:0007787Posterior subcapsular cataract0CHMP4B CL E G H128866605387Cataract, posterior polar, 3605387C1854311OMIM132116171610897
HP:0007787HP:0007787Posterior subcapsular cataract0GJA8 CL E G H2703116200Cataract 1116200C1861828OMIM1633474281600897
HP:0007787HP:0007787Posterior subcapsular cataract0IMPG2 CL E G H50939613581Retinitis pigmentosa 56613581C3150819OMIM14234618362607056
HP:0007787HP:0007787Posterior subcapsular cataract0OAT CL E G H4942258870Ornithine aminotransferase deficiency258870C0599035OMIM1722178091613349
HP:0007787HP:0007787Posterior subcapsular cataract0RBP3 CL E G H5949615233Retinitis pigmentosa 66615233C3715216OMIM1183779921180290
HP:0007787HP:0007787Posterior subcapsular cataract0REEP6 CL E G H92840617304Retinitis pigmentosa 77617304C4310626OMIM186930078609346
HP:0007787HP:0007787Posterior subcapsular cataract0SPRTN CL E G H83932616200Ruijs-Aalfs syndrome616200C4015461OMIM134625356616086
HP:0007787HP:0007787Posterior subcapsular cataract0ZNF408 CL E G H79797616469Retinitis pigmentosa 72616469C4225315OMIM11411220041616454
HP:0007787HP:0007787Posterior subcapsular cataract1CHMP4B CL E G H128866605387Cataract, posterior polar, 3605387C1854311OMIM132116171610897
HP:0007787HP:0007787Posterior subcapsular cataract1GJA8 CL E G H2703116200Cataract 1116200C1861828OMIM1633474281600897
HP:0007787HP:0007787Posterior subcapsular cataract1IMPG2 CL E G H50939613581Retinitis pigmentosa 56613581C3150819OMIM14234618362607056
HP:0007787HP:0007787Posterior subcapsular cataract1OAT CL E G H4942258870Ornithine aminotransferase deficiency258870C0599035OMIM1722178091613349
HP:0007787HP:0007787Posterior subcapsular cataract1RBP3 CL E G H5949615233Retinitis pigmentosa 66615233C3715216OMIM1183779921180290
HP:0007787HP:0007787Posterior subcapsular cataract1REEP6 CL E G H92840617304Retinitis pigmentosa 77617304C4310626OMIM186930078609346
HP:0007787HP:0007787Posterior subcapsular cataract1SPRTN CL E G H83932616200Ruijs-Aalfs syndrome616200C4015461OMIM134625356616086
HP:0007787HP:0007787Posterior subcapsular cataract1ZNF408 CL E G H79797616469Retinitis pigmentosa 72616469C4225315OMIM11411220041616454
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007787HP:0007787Posterior subcapsular cataract0ADAMTS18 CL E G H170692615458Microcornea, myopic chorioretinal atrophy, and telecanthus615458C3809567OMIM01719717110607512
HP:0007787HP:0007787Posterior subcapsular cataract0ARL2BP CL E G H23568615434Retinitis pigmentosa with or without situs inversus615434C3809503OMIM053517146615407
HP:0007787HP:0007787Posterior subcapsular cataract0EYS CL E G H346007602772Retinitis pigmentosa 25602772C1864446OMIM0338106421555612424
HP:0007787HP:0007787Posterior subcapsular cataract0IMPDH1 CL E G H3614180105Retinitis pigmentosa 10180105C1867299OMIM0241986052146690
HP:0007787HP:0007787Posterior subcapsular cataract0OFD1 CL E G H8481300424Retinitis Pigmentosa 23300424C1419610OMIM01625102567300170
HP:0007787HP:0007787Posterior subcapsular cataract0OPA3 CL E G H8020767036ORPHA0153188142606580
HP:0007787HP:0007787Posterior subcapsular cataract0TULP1 CL E G H7287600132Retinitis pigmentosa 14600132C1838603OMIM07520812423602280
HP:0007787HP:0007787Posterior subcapsular cataract1ADAMTS18 CL E G H170692615458Microcornea, myopic chorioretinal atrophy, and telecanthus615458C3809567OMIM01719717110607512
HP:0007787HP:0007787Posterior subcapsular cataract1ARL2BP CL E G H23568615434Retinitis pigmentosa with or without situs inversus615434C3809503OMIM053517146615407
HP:0007787HP:0007787Posterior subcapsular cataract1EYS CL E G H346007602772Retinitis pigmentosa 25602772C1864446OMIM0338106421555612424
HP:0007787HP:0007787Posterior subcapsular cataract1IMPDH1 CL E G H3614180105Retinitis pigmentosa 10180105C1867299OMIM0241986052146690
HP:0007787HP:0007787Posterior subcapsular cataract1OFD1 CL E G H8481300424Retinitis Pigmentosa 23300424C1419610OMIM01625102567300170
HP:0007787HP:0007787Posterior subcapsular cataract1OPA3 CL E G H8020767036ORPHA0153188142606580
HP:0007787HP:0007787Posterior subcapsular cataract1TULP1 CL E G H7287600132Retinitis pigmentosa 14600132C1838603OMIM07520812423602280


Genes (17) :ADAMTS18 ARL2BP CHMP4B CNBP EYS GJA8 IMPDH1 IMPG2 NF2 OAT OFD1 OPA3 RBP3 REEP6 SPRTN TULP1 ZNF408

Diseases (17) :615458 615434 605387 602772 116200 180105 613581 258870 300424 67036 615233 617304 616200 600132 616469 602668 101000
 

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