Human Phenotype Ontology 
Grandparent Node:
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Abnormal anterior eye segment morphology (HP:0004328)help
Parent Node:
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Abnormal cornea morphology (HP:0000481)help
..Starting node
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Decreased corneal sensation (HP:0012155)help
Term ID: 12155
Name: Decreased corneal sensation
Synonym: Corneal hypaesthesia; Corneal hypesthesia; Decreased corneal sensitivity; Reduced corneal sensation
Definition: Reduced ability of the cornea to respond to stimulation.
Comments:
Reference: HP:0012155
Genes and Diseases:
 
       Child Nodes:

 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 degeneration (HP:0007705) 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
..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:0012155HP:0012155Decreased corneal sensation0CHST6 CL E G H41666938ORPHA:98969Macular corneal dystrophyHP:0040283 - Occasional129
HP:0012155HP:0012155Decreased corneal sensation0FGF10 CL E G H22553666ORPHA:2363Lacrimoauriculodentodigital syndromeHP:0040283 - Occasional17
HP:0012155HP:0012155Decreased corneal sensation0FGFR2 CL E G H22633689ORPHA:2363Lacrimoauriculodentodigital syndromeHP:0040283 - Occasional175
HP:0012155HP:0012155Decreased corneal sensation0FGFR3 CL E G H22613690ORPHA:2363Lacrimoauriculodentodigital syndromeHP:0040283 - Occasional145
HP:0012155HP:0012155Decreased corneal sensation0TGFBI CL E G H704511771ORPHA:98964Lattice corneal dystrophy type IHP:0040283 - Occasional58


Genes (5) :CHST6 FGF10 FGFR2 FGFR3 TGFBI

Diseases (3) :ORPHA:98969 ORPHA:2363 ORPHA:98964
 

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