Human Phenotype Ontology 
Grandparent Node:
Abnormal conjugate eye movement (HP:0000549)help
Parent Node:
Strabismus (HP:0000486)help
..Starting node
Neurogenic strabismus (HP:0031775)help
Term ID: 31775
Name: Neurogenic strabismus
Synonym: Paralytic strabismus
Definition: An ocular deviation caused by a palsy to one or more of the extraocular muscles or nerves supplying them.
Reference: HP:0031775
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandConcomitant strabismus (HP:0025069) help
..expandCyclodeviation (HP:0025589) help
..expandEsodeviation (HP:0020045) help
..expandExodeviation (HP:0020049) help
..expandHyperdeviation (HP:0025587) help
..expandHypodeviation (HP:0025588) help
..expandIncomitant strabismus (HP:0025068) help
..expandMicrotropia (HP:0031724) help
..expandMonocular strabismus (HP:0010877) help
..expandobsolete Congenital strabismus (HP:0000487) 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:0031775HP:0031775Neurogenic strabismus0 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.