Human Phenotype Ontology 
Grandparent Node:
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Abnormality of ocular smooth pursuit (HP:0000617)help
Parent Node:
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Impaired smooth pursuit (HP:0007772)help
..Starting node
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Impaired horizontal smooth pursuit (HP:0001151)help
Term ID: 1151
Name: Impaired horizontal smooth pursuit
Synonym: Abnormal horizontal ocular pursuit; Impaired horizontal visual pursuit
Definition: An abnormality of ocular smooth pursuit characterized by an impairment of the ability to track horizontally moving objects.
Comments:
Reference: HP:0001151
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbsent smooth pursuit (HP:0007179) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0001151HP:0001151Impaired horizontal smooth pursuit0ATXN1 CL E G H6310164400Spinocerebellar ataxia 1164400C0752120OMIM1710548601556
HP:0001151HP:0001151Impaired horizontal smooth pursuit0ATXN2 CL E G H6311183090Spinocerebellar ataxia 2183090C0752121OMIM14410555601517
HP:0001151HP:0001151Impaired horizontal smooth pursuit0ATXN3 CL E G H4287109150Azorean disease109150C0024408OMIM137106607047
HP:0001151HP:0001151Impaired horizontal smooth pursuit0EEF2 CL E G H1938101112ORPHA143214130610
HP:0001151HP:0001151Impaired horizontal smooth pursuit0EEF2 CL E G H1938609306Spinocerebellar ataxia 26609306C1836395OMIM143214130610
HP:0001151HP:0001151Impaired horizontal smooth pursuit0POLR3B CL E G H55703614381Hypomyelinating leukodystrophy 8, with or without oligodontia and/or hypogonadotropic hypogonadism614381C3280644OMIM15830348614366
HP:0001151HP:0001151Impaired horizontal smooth pursuit0STXBP1 CL E G H6812612164Early infantile epileptic encephalopathy 4612164C2677326OMIM119511444602926
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (6) :ATXN1 ATXN2 ATXN3 EEF2 POLR3B STXBP1

Diseases (7) :164400 183090 109150 101112 609306 614381 612164
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.