Human Phenotype Ontology 
Grandparent Node:
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Zonular cataract (HP:0010920)help
Parent Node:
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Cortical cataract (HP:0100019)help
..Starting node
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Posterior cortical cataract (HP:0010924)help
Term ID: 10924
Name: Posterior cortical cataract
Synonym:
Definition: A cataract that affects the posterior part of the cortex of the lens.
Comments:
Reference: HP:0010924
Genes and Diseases:
 
       Child Nodes:
........expandDense posterior cortical cataract (HP:0007948) help

 Sister Nodes: 
..expandAnterior cortical cataract (HP:0007795) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010924HP:0010924Posterior cortical cataract0OCRL CL E G H49528108OMIM:309000Lowe syndrome88
HP:0010924HP:0010924Posterior cortical cataract0OPA3 CL E G H802078142ORPHA:67036Autosomal dominant optic atrophy and cataractHP:0040282 - Frequent163
HP:0010924HP:0010924Posterior cortical cataract0PANK4 CL E G H5522919366OMIM:619593CATARACT 49; CTRCT49
HP:0010924HP:0007948Dense posterior cortical cataract1OCRL CL E G H49528108OMIM:309000Lowe syndrome.88


Genes (3) :OCRL OPA3 PANK4

Diseases (3) :OMIM:309000 ORPHA:67036 OMIM:619593
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.