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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Hyperopic astigmatism (HP:0000484)help
Term ID: 484
Name: Hyperopic astigmatism
Synonym:
Definition: A form of astigmatism in which one meridian is hyperopic while the one at a right angle to it has no refractive error.
Comments:
Reference: HP:0000484
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAgainst the rule astigmatism (HP:0031789) help
..expandCorneal astigmatism (HP:0025612) 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:0000484HP:0000484Hyperopic astigmatism0CHST6 CL E G H41666938ORPHA:98969Macular corneal dystrophyHP:0040283 - Occasional129
HP:0000484HP:0000484Hyperopic astigmatism0GATAD2B CL E G H5745930778ORPHA:363686Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndromeHP:0040282 - Frequent33
HP:0000484HP:0000484Hyperopic astigmatism0GNPTAB CL E G H7915829670OMIM:252600Mucolipidosis III alpha/beta.240
HP:0000484HP:0000484Hyperopic astigmatism0GPR143 CL E G H493520145OMIM:300814Nystagmus 6, congenital, X-linked.64
HP:0000484HP:0000484Hyperopic astigmatism0ROBO3 CL E G H6422113433OMIM:607313Gaze palsy, familial horizontal, with progressive scoliosis, 190
HP:0000484HP:0000484Hyperopic astigmatism0TBC1D2B CL E G H2310229183ORPHA:397973Intellectual disability-obesity-prognathism-eye and skin anomalies syndromeHP:0040282 - Frequent


Genes (6) :CHST6 GATAD2B GNPTAB GPR143 ROBO3 TBC1D2B

Diseases (6) :ORPHA:98969 ORPHA:363686 OMIM:252600 OMIM:300814 OMIM:607313 ORPHA:397973
 

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