Human Phenotype Ontology 
Grandparent Node:
Abnormal oblique muscle physiology (HP:0031739)help
Parent Node:
Abnormal inferior oblique muscle physiology (HP:0025596)help
..Starting node
Inferior oblique muscle overaction (HP:0025599)help
Term ID: 25599
Name: Inferior oblique muscle overaction
Definition: A common ocular motility disorder characterized by vertical incomitance of the eyes in lateral gaze. In primary inferior oblique muscle overaction, an upshoot of the adducting eye occurs when gaze is directed into the field of action of the inferior oblique muscle, producing a greater upward excursion of the adducted eye than of the abducted eye.
Reference: HP:0025599
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandInferior oblique muscle weakness (HP:0025598) 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:0025599HP:0025599Inferior oblique muscle overaction0 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.