Human Phenotype Ontology 
Grandparent Node:
Abnormal horizontal rectus muscle physiology (HP:0031740)help
Parent Node:
Abnormal medial rectus muscle physiology (HP:0025606)help
..Starting node
Medial rectus muscle weakness (HP:0031753)help
Term ID: 31753
Name: Medial rectus muscle weakness
Definition: Decreased strength of the medial rectus muscle.
Reference: HP:0031753
Genes and Diseases:
       Child Nodes:
........expandMedial rectus muscle underaction (HP:0031756) help
........expandMedial rectus muscle restriction (HP:0031757) help

 Sister Nodes: 
..expandMedial rectus muscle overaction (HP:0031754) 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:0031753HP:0031753Medial rectus muscle weakness0 CL E G H
HP:0031753HP:0031757Medial rectus muscle restriction1 CL E G H
HP:0031753HP:0031756Medial rectus muscle underaction1 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.