Human Phenotype Ontology 
Grandparent Node:
expandAbnormal extraocular muscle physiology (HP:0025590)help
Parent Node:
expandAbnormal oblique muscle physiology (HP:0031739)help
..Starting node
..expandAbnormal inferior oblique muscle physiology (HP:0025596)help
Term ID: 25596
Name: Abnormal inferior oblique muscle physiology
Synonym:
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.
Comments:
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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025596HP:0025596Abnormal inferior oblique muscle physiology0FBN1 CL E G H22003603OMIM:154700Marfan syndrome1361
HP:0025596HP:0025598Inferior oblique muscle weakness1 CL E G H
HP:0025596HP:0025599Inferior oblique muscle overaction1FBN1 CL E G H22003603OMIM:154700Marfan syndrome1361
HP:0025596HP:0031741Inferior oblique muscle underaction2 CL E G H
HP:0025596HP:0025597Inferior oblique muscle restriction2 CL E G H


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.