Human Phenotype Ontology 
Grandparent Node:
Abnormal inferior rectus muscle physiology (HP:0025600)help
Parent Node:
Inferior rectus muscle weakness (HP:0025601)help
..Starting node
Inferior rectus muscle restriction (HP:0025602)help
Term ID: 25602
Name: Inferior rectus muscle restriction
Definition: Mechanical limitation of the range of movement of the inferior rectus muscle.
Reference: HP:0025602
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandInferior rectus muscle underaction (HP:0031742) 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:0025602HP:0025602Inferior rectus muscle restriction0 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.