Human Phenotype Ontology 
Grandparent Node:
Abnormality of eye movement (HP:0000496)help
Parent Node:
Abnormal involuntary eye movements (HP:0012547)help
..Starting node
Chaotic rapid conjugate ocular movements (HP:0007295)help
Term ID: 7295
Name: Chaotic rapid conjugate ocular movements
Reference: HP:0007295
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandNystagmus (HP:0000639) help
..expandOpsoclonus (HP:0010543) 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:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007295HP:0007295Chaotic rapid conjugate ocular movements0 CL E G H

Genes (0) :

Diseases (0) :

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