Human Phenotype Ontology 
Grandparent Node:
Abnormality of eye movement (HP:0000496)help
Parent Node:
Abnormal involuntary eye movements (HP:0012547)help
..Starting node
Opsoclonus (HP:0010543)help
Term ID: 10543
Name: Opsoclonus
Definition: Bursts of large-amplitude multidirectional saccades without intersaccadic interval
Reference: HP:0010543
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandChaotic rapid conjugate ocular movements (HP:0007295) help
..expandNystagmus (HP:0000639) help
..expandParoxysmal involuntary eye movements (HP:0007704) help
..expandUncontrolled eye movements (HP:0007738) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HP:0010543HP:0010543Opsoclonus0CLCN7 CL E G H1186667ORPHA15492025602727
HP:0010543HP:0010543Opsoclonus0CLCN7 CL E G H1186667ORPHA13882025602727
HP:0010543HP:0010543Opsoclonus0NME1 CL E G H4830256700Neuroblastoma256700C0027819OMIM1147849156490
HP:0010543HP:0010543Opsoclonus0SNX10 CL E G H29887667ORPHA18914974614780
HP:0010543HP:0010543Opsoclonus0SNX10 CL E G H29887667ORPHA15614974614780
HP:0010543HP:0010543Opsoclonus0TCIRG1 CL E G H10312667ORPHA167411647604592
HP:0010543HP:0010543Opsoclonus0TCIRG1 CL E G H10312667ORPHA154411647604592
HP:0010543HP:0010543Opsoclonus0TNFSF11 CL E G H8600667ORPHA116611926602642
HP:0010543HP:0010543Opsoclonus0TNFSF11 CL E G H8600667ORPHA112911926602642
HPO disease - gene - phenotype less frequent non-typical associations:

Genes (5) :CLCN7 NME1 SNX10 TCIRG1 TNFSF11

Diseases (2) :667 256700

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.