Human Phenotype Ontology 
Grandparent Node:
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Abnormality of eye movement (HP:0000496)help
Parent Node:
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Abnormality of ocular smooth pursuit (HP:0000617)help
..Starting node
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Jerky ocular pursuit movements (HP:0008003)help
Term ID: 8003
Name: Jerky ocular pursuit movements
Synonym: Jerky smooth pursuit
Definition:
Comments:
Reference: HP:0008003
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandImpaired pursuit initiation and maintenance (HP:0007668) help
..expandImpaired smooth pursuit (HP:0007772) help
..expandSaccadic smooth pursuit (HP:0001152) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0008003HP:0008003Jerky ocular pursuit movements0GBA2 CL E G H57704614409Spastic paraplegia 46, autosomal recessive614409C2828721OMIM12318986609471
HP:0008003HP:0008003Jerky ocular pursuit movements0KCNC3 CL E G H3748605259Spinocerebellar ataxia 13605259C1854488OMIM1126235176264
HP:0008003HP:0008003Jerky ocular pursuit movements0TTBK2 CL E G H14605798767ORPHA11119141611695
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008003HP:0008003Jerky ocular pursuit movements0GBA2 CL E G H57704320391ORPHA02318986609471
HP:0008003HP:0008003Jerky ocular pursuit movements0KCNC3 CL E G H374898768ORPHA0126235176264
HP:0008003HP:0008003Jerky ocular pursuit movements0PRNP CL E G H5621157941ORPHA01099449176640
HP:0008003HP:0008003Jerky ocular pursuit movements0SPTBN2 CL E G H6712352403ORPHA02911276604985
HP:0008003HP:0008003Jerky ocular pursuit movements0SPTBN2 CL E G H6712615386Spinocerebellar ataxia, autosomal recessive 14615386C3809327OMIM02911276604985


Genes (5) :GBA2 KCNC3 PRNP SPTBN2 TTBK2

Diseases (8) :320391 614409 98768 605259 157941 352403 615386 98767
 

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