Human Phenotype Ontology 
Grandparent Node:
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Abnormal cornea morphology (HP:0000481)help
Parent Node:
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Abnormal corneal endothelium morphology (HP:0011488)help
..Starting node
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Reduced number of corneal endothelial cells (HP:0011491)help
Term ID: 11491
Name: Reduced number of corneal endothelial cells
Synonym:
Definition: A reduction in the number of corneal endothelial cells.
Comments:
Reference: HP:0011491
Genes and Diseases:
 
       Child Nodes:
........expandPolymorphous posterior corneal dystrophy (HP:0007915) help

 Sister Nodes: 
..expandAbnormal Descemet membrane morphology (HP:0011490) help
..expandAbnormal migration of corneal endothelium (HP:0011489) help
..expandCorneal keratic precipitates (HP:0025341) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011491HP:0011491Reduced number of corneal endothelial cells0 CL E G H
HP:0011491HP:0011491Reduced number of corneal endothelial cells1 CL E G H


Genes (1) :OVOL2

Diseases (1) :122000
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.