Human Phenotype Ontology 
Grandparent Node:
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Abnormal oblique muscle physiology (HP:0031739)help
Parent Node:
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Abnormal inferior oblique muscle physiology (HP:0025596)help
..Starting node
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Inferior oblique muscle weakness (HP:0025598)help
Term ID: 25598
Name: Inferior oblique muscle weakness
Synonym: Inferior oblique palsy
Definition: Decreased strength of the inferior oblique muscle.
Comments:
Reference: HP:0025598
Genes and Diseases:
 
       Child Nodes:
........expandInferior oblique muscle restriction (HP:0025597) help
........expandInferior oblique muscle underaction (HP:0031741) help

 Sister Nodes: 
..expandInferior oblique muscle overaction (HP:0025599) 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:0025598HP:0025598Inferior oblique muscle weakness0 CL E G H
HP:0025598HP:0031741Inferior oblique muscle underaction1 CL E G H
HP:0025598HP:0025597Inferior oblique 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.