Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of refraction (HP:0000539)help
Grandparent Node:
expandAbnormality of the curvature of the cornea (HP:0100691)help
Parent Node:
expandAstigmatism (HP:0000483)help
..Starting node
..expandWith the rule astigmatism (HP:0031788)help
Term ID: 31788
Name: With the rule astigmatism
Synonym:
Definition: Refractive error in which the vertical meridian is relatively hypermetropic and the horizontal meridian is relatively myopic (or ocular astigmatism in which the refractive power of the horizontal meridian is the greatest).
Comments:
Reference: HP:0031788
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAgainst the rule astigmatism (HP:0031789) help
..expandCorneal astigmatism (HP:0025612) 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
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031788HP:0031788With the rule astigmatism0 CL E G H


Genes (0) :

Diseases (0) :
 

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