Human Phenotype Ontology 
Grandparent Node:
Abnormality of eye movement (HP:0000496)help
Parent Node:
Abnormal involuntary eye movements (HP:0012547)help
..Starting node
Uncontrolled eye movements (HP:0007738)help
Term ID: 7738
Name: Uncontrolled eye movements
Reference: HP:0007738
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandChaotic rapid conjugate ocular movements (HP:0007295) help
..expandNystagmus (HP:0000639) help
..expandOpsoclonus (HP:0010543) help
..expandParoxysmal involuntary eye movements (HP:0007704) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HP:0007738HP:0007738Uncontrolled eye movements0POMGNT1 CL E G H55624253280Muscle eye brain disease253280C0457133OMIM18919139606822
HPO disease - gene - phenotype less frequent non-typical associations:

Genes (1) :POMGNT1

Diseases (1) :253280

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