Human Phenotype Ontology 
Grandparent Node:
Abnormal rectus muscle physiology (HP:0031755)help
Parent Node:
Abnormal horizontal rectus muscle physiology (HP:0031740)help
..Starting node
Abnormal medial rectus muscle physiology (HP:0025606)help
Term ID: 25606
Name: Abnormal medial rectus muscle physiology
Definition: A functional anomaly of the medial rectus muscle, an extraocular muscle that is innervated by the inferior division of the oculomotor nerve and whose sole action is the adduction of the eyeball.
Reference: HP:0025606
Genes and Diseases:
       Child Nodes:
........expandMedial rectus muscle weakness (HP:0031753) help
................... HP:0031756 Medial rectus muscle underaction
................... HP:0031757 Medial rectus muscle restriction
........expandMedial rectus muscle overaction (HP:0031754) help

 Sister Nodes: 
..expandAbnormal lateral rectus muscle physiology (HP:0031749) 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:0025606HP:0025606Abnormal medial rectus muscle physiology0 CL E G H
HP:0025606HP:0031754Medial rectus muscle overaction1 CL E G H
HP:0025606HP:0031753Medial rectus muscle weakness1 CL E G H
HP:0025606HP:0031756Medial rectus muscle underaction2 CL E G H
HP:0025606HP:0031757Medial rectus 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 December 15 2022 release.