Human Phenotype Ontology 
Grandparent Node:
Abnormal inferior oblique muscle physiology (HP:0025596)help
Parent Node:
Inferior oblique muscle weakness (HP:0025598)help
..Starting node
Inferior oblique muscle underaction (HP:0031741)help
Term ID: 31741
Name: Inferior oblique muscle underaction
Definition: Reduced ocular movement by the inferior oblique muscle which improves on testing ductions, typically associated with neurogenic palsy.
Reference: HP:0031741
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandInferior oblique muscle restriction (HP:0025597) 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:0031741HP:0031741Inferior oblique muscle underaction0 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.