Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal oblique muscle physiology (HP:0031739)help
Parent Node:
expand
Abnormal inferior oblique muscle physiology (HP:0025596)help
..Starting node
..expand
Inferior oblique muscle overaction (HP:0025599)help
Term ID: 25599
Name: Inferior oblique muscle overaction
Synonym:
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.
Comments:
Reference: HP:0025599
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandInferior oblique muscle weakness (HP:0025598) 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:0025599HP:0025599Inferior oblique muscle overaction0FBN1 CL E G H22003603OMIM:154700Marfan syndrome1361


Genes (1) :FBN1

Diseases (1) :OMIM:154700
 

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