Human Phenotype Ontology 
Grandparent Node:
Abnormal involuntary eye movements (HP:0012547)help
Parent Node:
Abnormality of the vestibulocochlear nerve (HP:0009591)help
Parent Node:
Nystagmus (HP:0000639)help
..Starting node
Vestibular nystagmus (HP:0010542)help
Term ID: 10542
Name: Vestibular nystagmus
Definition: Nystagmus due to disturbance of the vestibular system; eye movements are rhythmic, with slow and fast components.
Reference: HP:0010542
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandCongenital nystagmus (HP:0006934) help
..expandDivergence nystagmus (HP:0030691) help
..expandGaze-evoked nystagmus (HP:0000640) help
..expandHorizontal nystagmus (HP:0000666) help
..expandNystagmus-induced head nodding (HP:0001361) help
..expandPendular nystagmus (HP:0012043) help
..expandRotary nystagmus (HP:0001583) help
..expandVertical nystagmus (HP:0010544) 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:0010542HP:0010542Vestibular nystagmus0PRNP CL E G H5621282166ORPHA01099449176640

Genes (1) :PRNP

Diseases (1) :282166

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.