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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Uncontrolled eye movements (HP:0007738)help
Term ID: 7738
Name: Uncontrolled eye movements
Synonym:
Definition:
Comments:
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 disease253280C0457133OMIM179719139606822
HP:0007738HP:0007738Uncontrolled eye movements0POMGNT1 CL E G H55624253280Muscle eye brain disease253280C0457133OMIM166219139606822
 
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 August 2021 release.