Human Phenotype Ontology 
Grandparent Node:
expandAbnormal rectus muscle physiology (HP:0031755)help
Parent Node:
expandAbnormal vertical rectus muscle physiology (HP:0031748)help
..Starting node
..expandAbnormal inferior rectus muscle physiology (HP:0025600)help
Term ID: 25600
Name: Abnormal inferior rectus muscle physiology
Synonym:
Definition: A functional anomaly of the inferior rectus muscle, which is innervated by the inferior division of oculomotor nerve and functions in the depression, adduction, and lateral rotation (extortion) of the eye.
Comments:
Reference: HP:0025600
Genes and Diseases:
 
       Child Nodes:
........expandInferior rectus muscle weakness (HP:0025601) help
................... HP:0025602 Inferior rectus muscle restriction
................... HP:0031742 Inferior rectus muscle underaction
........expandInferior rectus muscle overaction (HP:0031743) help

 Sister Nodes: 
..expandAbnormal superior rectus muscle physiology (HP:0025603) 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:0025600HP:0025600Abnormal inferior rectus muscle physiology0 CL E G H
HP:0025600HP:0031743Inferior rectus muscle overaction1 CL E G H
HP:0025600HP:0025601Inferior rectus muscle weakness1 CL E G H
HP:0025600HP:0031742Inferior rectus muscle underaction2 CL E G H
HP:0025600HP:0025602Inferior 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.