Human Phenotype Ontology 
Grandparent Node:
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Abnormal corneal stroma morphology (HP:0011492)help
Grandparent Node:
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Corneal opacity (HP:0007957)help
Parent Node:
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Opacification of the corneal stroma (HP:0007759)help
..Starting node
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Generalized opacification of the cornea (HP:0011494)help
Term ID: 11494
Name: Generalized opacification of the cornea
Synonym: Generalised opacification of the cornea
Definition: Generalized reduced transparency of the stroma of the cornea.
Comments:
Reference: HP:0011494
Genes and Diseases:
 
       Child Nodes:
........expandNodular corneal dystrophy (HP:0007827) help

 Sister Nodes: 
..expandCentral opacification of the cornea (HP:0011493) help
..expandCorneal crystals (HP:0000531) help
..expandPeripheral opacification of the cornea (HP:0008011) help
..expandPunctate opacification of the cornea (HP:0007856) 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:0011494HP:0011494Generalized opacification of the cornea0TGFBI CL E G H704511771OMIM:121900Groenouw type I corneal dystrophy58
HP:0011494HP:0007827Nodular corneal dystrophy1TGFBI CL E G H704511771OMIM:121900Groenouw type I corneal dystrophy.58


Genes (1) :TGFBI

Diseases (1) :OMIM:121900
 

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