Human Phenotype Ontology 
Grandparent Node:
expandAbnormal anterior eye segment morphology (HP:0004328)help
Parent Node:
expandAbnormal cornea morphology (HP:0000481)help
..Starting node
..expandCorneal degeneration (HP:0007705)help
Term ID: 7705
Name: Corneal degeneration
Synonym:
Definition:
Comments:
Reference: HP:0007705
Genes and Diseases:
 
       Child Nodes:
........expandRibbonlike corneal degeneration (HP:0200066) help

 Sister Nodes: 
..expandAbnormal corneal endothelium morphology (HP:0011488) help
..expandAbnormal corneal epithelium morphology (HP:0011495) help
..expandAbnormal corneal limbus morphology (HP:0025348) help
..expandAbnormal corneal stroma morphology (HP:0011492) help
..expandAbnormal line of Schwalbe morphology (HP:0008048) help
..expandAbnormality of corneal shape (HP:0040004) help
..expandAbnormality of corneal size (HP:0001120) help
..expandAbnormality of corneal thickness (HP:0011486) help
..expandAbnormality of the curvature of the cornea (HP:0100691) help
..expandCornea verticillata (HP:0500008) help
..expandCorneal dystrophy (HP:0001131) help
..expandCorneal neovascularization (HP:0011496) help
..expandCorneal opacity (HP:0007957) help
..expandCorneal perforation (HP:0100583) help
..expandDecreased corneal reflex (HP:0008000) help
..expandDecreased corneal sensation (HP:0012155) help
..expandLimbal dermoid (HP:0001140) 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:0007705HP:0007705Corneal degeneration0COL8A2 CL E G H12962216OMIM:136800Corneal dystrophy, fuchs endothelial, 1.3
HP:0007705HP:0200066Ribbonlike corneal degeneration1 CL E G H


Genes (1) :COL8A2

Diseases (1) :OMIM:136800
 

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