Human Phenotype Ontology 
Grandparent Node:
Abnormal rectus muscle physiology (HP:0031755)help
Parent Node:
Abnormal vertical rectus muscle physiology (HP:0031748)help
..Starting node
Abnormal superior rectus muscle physiology (HP:0025603)help
Term ID: 25603
Name: Abnormal superior rectus muscle physiology
Definition: A functional anomaly of the superior rectus muscle, an extraocular muscle that is innervated by the superior division of the oculomotor nerve, and whose primary function is the elevation of the globe.
Reference: HP:0025603
Genes and Diseases:
       Child Nodes:
........expandSuperior rectus muscle weakness (HP:0031744) help
................... HP:0031746 Superior rectus muscle rescriction
................... HP:0031747 Superior rectus muscle underaction
........expandSuperior rectus muscle overaction (HP:0031745) help

 Sister Nodes: 
..expandAbnormal inferior rectus muscle physiology (HP:0025600) 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:0025603HP:0025603Abnormal superior rectus muscle physiology0 CL E G H
HP:0025603HP:0031744Superior rectus muscle weakness1 CL E G H
HP:0025603HP:0031745Superior rectus muscle overaction1 CL E G H
HP:0025603HP:0031746Superior rectus muscle restriction2 CL E G H
HP:0025603HP:0031747Superior rectus muscle underaction2 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.