Human Phenotype Ontology 
Grandparent Node:
Abnormal extraocular muscle physiology (HP:0025590)help
Parent Node:
Abnormal oblique muscle physiology (HP:0031739)help
..Starting node
Abnormal inferior oblique muscle physiology (HP:0025596)help
Term ID: 25596
Name: Abnormal inferior oblique muscle physiology
Definition: A functional anomaly of the inferior oblique muscle, an extraocular muscle that has its origin on the maxillary bone just posterior to the inferior medial orbital rim and lateral to the nasolacrimal canal and that is innervated by the inferior branch of the oculomotor nerve.
Reference: HP:0025596
Genes and Diseases:
       Child Nodes:
........expandInferior oblique muscle weakness (HP:0025598) help
................... HP:0025597 Inferior oblique muscle restriction
................... HP:0031741 Inferior oblique muscle underaction
........expandInferior oblique muscle overaction (HP:0025599) help

 Sister Nodes: 
..expandAbnormal superior oblique muscle physiology (HP:0025591) 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:0025596HP:0025596Abnormal inferior oblique muscle physiology0 CL E G H
HP:0025596HP:0025598Inferior oblique muscle weakness1 CL E G H
HP:0025596HP:0025599Inferior oblique muscle overaction1 CL E G H
HP:0025596HP:0031741Inferior oblique muscle underaction2 CL E G H
HP:0025596HP:0025597Inferior oblique muscle restriction2 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.