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
..expandMixed astigmatism (HP:0031790)help
Term ID: 31790
Name: Mixed astigmatism
Synonym:
Definition: A type of astigmatism in which an unequal curvature of the cornea and some cases additionally of the lens causes one meridian of the eye to be hyperopic (farsighted) and a second meridian that is perpendicular to the first to be myopic (nearsighted).
Comments:
Reference: HP:0031790
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
..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:0031790HP:0031790Mixed astigmatism0AGBL5 CL E G H6050926147OMIM:617023Retinitis pigmentosa 75.2


Genes (1) :AGBL5

Diseases (1) :OMIM:617023
 

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