Human Phenotype Ontology 
Grandparent Node:
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Abnormality of eye movement (HP:0000496)help
Parent Node:
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Abnormal involuntary eye movements (HP:0012547)help
..Starting node
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Chaotic rapid conjugate ocular movements (HP:0007295)help
Term ID: 7295
Name: Chaotic rapid conjugate ocular movements
Synonym:
Definition:
Comments:
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.