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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007738HP:0007738Uncontrolled eye movements0ADORA2A CL E G H135263ORPHA:363549Acute encephalopathy with biphasic seizures and late reduced diffusionHP:0040283 - Occasional1
HP:0007738HP:0007738Uncontrolled eye movements0CACNA1H CL E G H89121395ORPHA:64280Childhood absence epilepsyHP:0040283 - Occasional75
HP:0007738HP:0007738Uncontrolled eye movements0GABRA1 CL E G H25544075ORPHA:64280Childhood absence epilepsyHP:0040283 - Occasional134
HP:0007738HP:0007738Uncontrolled eye movements0GABRB3 CL E G H25624083ORPHA:64280Childhood absence epilepsyHP:0040283 - Occasional57
HP:0007738HP:0007738Uncontrolled eye movements0GABRG2 CL E G H25664087ORPHA:64280Childhood absence epilepsyHP:0040283 - Occasional139
HP:0007738HP:0007738Uncontrolled eye movements0JRK CL E G H86296199ORPHA:64280Childhood absence epilepsyHP:0040283 - Occasional
HP:0007738HP:0007738Uncontrolled eye movements0POMGNT1 CL E G H5562419139OMIM:253280Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3.180
HP:0007738HP:0007738Uncontrolled eye movements0SLC2A1 CL E G H651311005ORPHA:64280Childhood absence epilepsyHP:0040283 - Occasional255


Genes (8) :ADORA2A CACNA1H GABRA1 GABRB3 GABRG2 JRK POMGNT1 SLC2A1

Diseases (3) :ORPHA:363549 ORPHA:64280 OMIM:253280
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.