Human Phenotype Ontology 
Grandparent Node:
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Ataxia (HP:0001251)help
Parent Node:
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Dyssynergia (HP:0010867)help
..Starting node
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Ocular dyssynergia (HP:0010868)help
Term ID: 10868
Name: Ocular dyssynergia
Synonym:
Definition: A type of dyssynergia affecting eye movements and characterized by the inability to smoothly follow a visual target across the visual field.
Comments:
Reference: HP:0010868
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAsynergia (HP:0010869) 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:0010868HP:0010868Ocular dyssynergia0 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.