Human Phenotype Ontology 
Grandparent Node:
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Subcapsular cataract (HP:0000523)help
Parent Node:
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Posterior subcapsular cataract (HP:0007787)help
..Starting node
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Juvenile posterior subcapsular lenticular opacities (HP:0007935)help
Term ID: 7935
Name: Juvenile posterior subcapsular lenticular opacities
Synonym:
Definition:
Comments:
Reference: HP:0007935
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandIridescent posterior subcapsular cataract (HP:0007889) 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:0007935HP:0007935Juvenile posterior subcapsular lenticular opacities0NF2 CL E G H47717773OMIM:101000Neurofibromatosis, type II220


Genes (1) :NF2

Diseases (1) :OMIM:101000
 

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