Human Phenotype Ontology 
Grandparent Node:
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Abnormality of refraction (HP:0000539)help
Grandparent Node:
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Abnormality of the curvature of the cornea (HP:0100691)help
Parent Node:
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Astigmatism (HP:0000483)help
..Starting node
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Corneal astigmatism (HP:0025612)help
Term ID: 25612
Name: Corneal astigmatism
Synonym:
Definition: A type of refractive error related abnormal curvatures on the anterior or posterior surface of the cornea.
Comments:
Reference: HP:0025612
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAgainst the rule astigmatism (HP:0031789) help
..expandHyperopic astigmatism (HP:0000484) help
..expandIrregular astigmatism (HP:0031792) help
..expandLenticular astigmatism (HP:0031791) help
..expandMixed astigmatism (HP:0031790) help
..expandMyopic astigmatism (HP:0500041) help
..expandOblique astigmatism (HP:0031787) help
..expandWith the rule astigmatism (HP:0031788) 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:0025612HP:0025612Corneal astigmatism0PITX2 CL E G H53089005OMIM:180550Ring dermoid of cornea51


Genes (1) :PITX2

Diseases (1) :OMIM:180550
 

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