Human Phenotype Ontology 
Grandparent Node:
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Abnormality of ocular smooth pursuit (HP:0000617)help
Parent Node:
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Saccadic smooth pursuit (HP:0001152)help
..Starting node
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Microsaccadic pursuit (HP:0007792)help
Term ID: 7792
Name: Microsaccadic pursuit
Synonym:
Definition:
Comments:
Reference: HP:0007792
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandIntermittent microsaccadic pursuits (HP:0007944) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007792HP:0007792Microsaccadic pursuit0TMEM240 CL E G H339453607454Spinocerebellar ataxia 21607454C1843891OMIM1625186616101
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :TMEM240

Diseases (1) :607454
 

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