Human Phenotype Ontology 
Grandparent Node:
Abnormality of ocular smooth pursuit (HP:0000617)help
Parent Node:
Saccadic smooth pursuit (HP:0001152)help
..Starting node
Intermittent microsaccadic pursuits (HP:0007944)help
Term ID: 7944
Name: Intermittent microsaccadic pursuits
Reference: HP:0007944
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandMicrosaccadic pursuit (HP:0007792) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HP:0007944HP:0007944Intermittent microsaccadic pursuits0KCND3 CL E G H3752607346Spinocerebellar ataxia 19607346C1846367OMIM1296239605411
HP:0007944HP:0007944Intermittent microsaccadic pursuits0TMEM240 CL E G H33945398773ORPHA1625186616101
HPO disease - gene - phenotype less frequent non-typical associations:

Genes (2) :KCND3 TMEM240

Diseases (2) :607346 98773

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