Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the eye (HP:0000478)help
Parent Node:
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Abnormal eye physiology (HP:0012373)help
..Starting node
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Staring gaze (HP:0025401)help
Term ID: 25401
Name: Staring gaze
Synonym: Staring eyes
Definition: An abnormality in which the eyes are held permanently wide open.
Comments:
Reference: HP:0025401
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal extraocular muscle physiology (HP:0025590) help
..expandAbnormal eyelid physiology (HP:0031879) help
..expandAbnormal intraocular pressure (HP:0012632) help
..expandAbnormal pupillary function (HP:0007686) help
..expandAbnormal visual accommodation (HP:0030800) help
..expandAbnormal visual electrophysiology (HP:0030453) help
..expandAbnormality of eye movement (HP:0000496) help
..expandAbnormality of refraction (HP:0000539) help
..expandAbnormality of vision (HP:0000504) help
..expandAsthenopia (HP:0031590) help
..expandCongenital stationary cone dysfunction (HP:0030637) help
..expandGlaucoma (HP:0000501) help
..expandHemorrhage of the eye (HP:0011885) help
..expandInflammatory abnormality of the eye (HP:0100533) help
..expandLacrimation abnormality (HP:0000632) help
..expandOcular pain (HP:0200026) help
..expandPtosis (HP:0000508) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0025401HP:0025401Staring gaze0ATXN1 CL E G H631098755ORPHA177410548601556
HP:0025401HP:0025401Staring gaze0SYNJ1 CL E G H8867615530Parkinson disease 20, early-onset615530C3809824OMIM12772311503604297
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025401HP:0025401Staring gaze0AGRN CL E G H37579098914ORPHA0181303329103320
HP:0025401HP:0025401Staring gaze0CHAT CL E G H110398914ORPHA0775001912118490
HP:0025401HP:0025401Staring gaze0COL13A1 CL E G H130598914ORPHA031752190120350
HP:0025401HP:0025401Staring gaze0MYO9A CL E G H464998914ORPHA061647608604875
HP:0025401HP:0025401Staring gaze0PNKD CL E G H2595398810Paroxysmal non-kinesigenic dyskinesiaC1869117ORPHA053319153609023
HP:0025401HP:0025401Staring gaze0PRRT2 CL E G H11247698810Paroxysmal non-kinesigenic dyskinesiaC1869117ORPHA010558930500614386
HP:0025401HP:0025401Staring gaze0SLC18A3 CL E G H657298914ORPHA069810936600336
HP:0025401HP:0025401Staring gaze0SLC25A1 CL E G H657698914ORPHA02446310979190315
HP:0025401HP:0025401Staring gaze0SLC5A7 CL E G H6048298914ORPHA02025814025608761
HP:0025401HP:0025401Staring gaze0SNAP25 CL E G H661698914ORPHA0712311132600322
HP:0025401HP:0025401Staring gaze0SYT2 CL E G H12783398914ORPHA037511510600104
HP:0025401HP:0025401Staring gaze0VAMP1 CL E G H684398914ORPHA068212642185880


Genes (14) :AGRN ATXN1 CHAT COL13A1 MYO9A PNKD PRRT2 SLC18A3 SLC25A1 SLC5A7 SNAP25 SYNJ1 SYT2 VAMP1

Diseases (4) :98914 98755 98810 615530
 

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