Human Phenotype Ontology 
Grandparent Node:
Abnormal vertical rectus muscle physiology (HP:0031748)help
Parent Node:
Abnormal inferior rectus muscle physiology (HP:0025600)help
..Starting node
Inferior rectus muscle weakness (HP:0025601)help
Term ID: 25601
Name: Inferior rectus muscle weakness
Definition: Decreased strength of the inferior rectus muscle.
Reference: HP:0025601
Genes and Diseases:
       Child Nodes:
........expandInferior rectus muscle restriction (HP:0025602) help
........expandInferior rectus muscle underaction (HP:0031742) help

 Sister Nodes: 
..expandInferior rectus muscle overaction (HP:0031743) 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:0025601HP:0025601Inferior rectus muscle weakness0 CL E G H
HP:0025601HP:0031742Inferior rectus muscle underaction1 CL E G H
HP:0025601HP:0025602Inferior rectus muscle restriction1 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.