Human Phenotype Ontology 
Grandparent Node:
expandOphthalmoparesis (HP:0000597)help
Parent Node:
expandOphthalmoplegia (HP:0000602)help
..Starting node
..expandInternuclear ophthalmoplegia (HP:0030773)help
Term ID: 30773
Name: Internuclear ophthalmoplegia
Synonym:
Definition: An abnormality of conjugate lateral gaze in which the affected eye shows impairment of adduction. The pathognomonic clinical sign of internuclear ophthalmoplegia is an impaired adduction while testing horizontal saccades on the side of the lesion in the ipsilateral medial longitudinal fascicule.
Comments:
Reference: HP:0030773
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandExternal ophthalmoplegia (HP:0000544) help
..expandInternal ophthalmoplegia (HP:0007942) help
..expandProgressive ophthalmoplegia (HP:0007650) help
..expandSupranuclear ophthalmoplegia (HP:0000623) help
..expandTotal ophthalmoplegia (HP:0007824) 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:0030773HP:0030773Internuclear ophthalmoplegia0 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.