Human Phenotype Ontology 
Grandparent Node:
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Cataract (HP:0000518)help
Parent Node:
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Zonular cataract (HP:0010920)help
..Starting node
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Lamellar cataract (HP:0007971)help
Term ID: 7971
Name: Lamellar cataract
Synonym:
Definition: A congenital cataract in which opacity is limited to layers of the lens external to the nucleus (i.e., the perinuclear region), i.e., between the nuclear and cortical layers of the lens.
Comments:
Reference: HP:0007971
Genes and Diseases:
 
       Child Nodes:
........expandLamellar pulverulent cataract (HP:0010694) help
........expandLamellar cataract with riders (HP:0025558) help

 Sister Nodes: 
..expandCoralliform cataract (HP:0010921) help
..expandCoronary cataract (HP:0025559) help
..expandCortical cataract (HP:0100019) help
..expandNuclear cataract (HP:0100018) help
..expandPunctate cataract (HP:0007648) help
..expandSutural cataract (HP:0010695) 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:0007971HP:0007971Lamellar cataract0BFSP1 CL E G H6311040OMIM:611391Cataract 33, multiple types.15
HP:0007971HP:0007971Lamellar cataract0CRYBA4 CL E G H14132396OMIM:610425CATARACT 23, MULTIPLE TYPES; CTRCT2310
HP:0007971HP:0007971Lamellar cataract0HSF4 CL E G H32995227OMIM:116800Cataract, lamellar38
HP:0007971HP:0007971Lamellar cataract0MIP CL E G H42847103OMIM:615274Cataract 15, multiple types.40
HP:0007971HP:0025558Lamellar cataract with riders1 CL E G H
HP:0007971HP:0010694Lamellar pulverulent cataract1 CL E G H


Genes (4) :BFSP1 CRYBA4 HSF4 MIP

Diseases (4) :OMIM:611391 OMIM:610425 OMIM:116800 OMIM:615274
 

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