Human Phenotype Ontology 
Grandparent Node:
expand
Abnormality of eye movement (HP:0000496)help
Parent Node:
expand
Abnormal saccadic eye movements (HP:0000570)help
..Starting node
..expand
Hypometric saccades (HP:0000571)help
Term ID: 571
Name: Hypometric saccades
Synonym:
Definition: Saccadic undershoot, i.e., a saccadic eye movement that has less than the magnitude that would be required to gain fixation of the object.
Comments:
Reference: HP:0000571
Genes and Diseases:
 
       Child Nodes:
........expandHypometric horizontal saccades (HP:0007975) help
........expandHypometric upward saccades (HP:0031833) help

 Sister Nodes: 
..expandDysmetric saccades (HP:0000641) help
..expandHypermetric saccades (HP:0007338) help
..expandSlow saccadic eye movements (HP:0000514) help
..expandSquare-wave jerks (HP:0025402) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0000571HP:0000571Hypometric saccades0APTX CL E G H54840208920Ataxia-oculomotor apraxia type 1208920C1859598OMIM125815984606350
HP:0000571HP:0000571Hypometric saccades0APTX CL E G H54840208920Ataxia-oculomotor apraxia type 1208920C1859598OMIM123615984606350
HP:0000571HP:0000571Hypometric saccades0GRM1 CL E G H2911324262ORPHA11934593604473
HP:0000571HP:0000571Hypometric saccades0GRM1 CL E G H2911324262ORPHA11864593604473
HP:0000571HP:0000571Hypometric saccades0GRM1 CL E G H2911614831Spinocerebellar ataxia, autosomal recessive 13614831C3553816OMIM11934593604473
HP:0000571HP:0000571Hypometric saccades0GRM1 CL E G H2911614831Spinocerebellar ataxia, autosomal recessive 13614831C3553816OMIM11864593604473
HP:0000571HP:0000571Hypometric saccades0MME CL E G H4311497764ORPHA13427154120520
HP:0000571HP:0000571Hypometric saccades0MME CL E G H4311497764ORPHA11967154120520
HP:0000571HP:0000571Hypometric saccades0MRE11 CL E G H4361604391Ataxia-telangiectasia-like disorder 1604391C1858391OMIM112597230600814
HP:0000571HP:0000571Hypometric saccades0MRE11 CL E G H4361604391Ataxia-telangiectasia-like disorder 1604391C1858391OMIM112587230600814
HP:0000571HP:0000571Hypometric saccades0NKX6-2 CL E G H84504527497ORPHA115119321605955
HP:0000571HP:0000571Hypometric saccades0NKX6-2 CL E G H84504527497ORPHA111919321605955
HP:0000571HP:0000571Hypometric saccades0NKX6-2 CL E G H84504617560SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY617560C4479653OMIM115119321605955
HP:0000571HP:0000571Hypometric saccades0NKX6-2 CL E G H84504617560SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY617560C4479653OMIM111919321605955
HP:0000571HP:0000571Hypometric saccades0NPHP1 CL E G H4867609583Joubert syndrome 4609583C1846790OMIM16267905607100
HP:0000571HP:0000571Hypometric saccades0NPHP1 CL E G H4867609583Joubert syndrome 4609583C1846790OMIM15327905607100
HP:0000571HP:0000571Hypometric saccades0PLA2G6 CL E G H8398199351ORPHA15139039603604
HP:0000571HP:0000571Hypometric saccades0PLA2G6 CL E G H8398199351ORPHA14319039603604
HP:0000571HP:0031833Hypometric upward saccades1APTX CL E G H54840208920Ataxia-oculomotor apraxia type 1208920C1859598OMIM125815984606350
HP:0000571HP:0031833Hypometric upward saccades1APTX CL E G H54840208920Ataxia-oculomotor apraxia type 1208920C1859598OMIM123615984606350
HP:0000571HP:0007975Hypometric horizontal saccades1APTX CL E G H54840208920Ataxia-oculomotor apraxia type 1208920C1859598OMIM125815984606350
HP:0000571HP:0007975Hypometric horizontal saccades1APTX CL E G H54840208920Ataxia-oculomotor apraxia type 1208920C1859598OMIM123615984606350
HP:0000571HP:0031833Hypometric upward saccades1GRM1 CL E G H2911324262ORPHA11934593604473
HP:0000571HP:0031833Hypometric upward saccades1GRM1 CL E G H2911324262ORPHA11864593604473
HP:0000571HP:0007975Hypometric horizontal saccades1GRM1 CL E G H2911324262ORPHA11934593604473
HP:0000571HP:0007975Hypometric horizontal saccades1GRM1 CL E G H2911324262ORPHA11864593604473
HP:0000571HP:0031833Hypometric upward saccades1GRM1 CL E G H2911614831Spinocerebellar ataxia, autosomal recessive 13614831C3553816OMIM11934593604473
HP:0000571HP:0031833Hypometric upward saccades1GRM1 CL E G H2911614831Spinocerebellar ataxia, autosomal recessive 13614831C3553816OMIM11864593604473
HP:0000571HP:0007975Hypometric horizontal saccades1GRM1 CL E G H2911614831Spinocerebellar ataxia, autosomal recessive 13614831C3553816OMIM11934593604473
HP:0000571HP:0007975Hypometric horizontal saccades1GRM1 CL E G H2911614831Spinocerebellar ataxia, autosomal recessive 13614831C3553816OMIM11864593604473
HP:0000571HP:0031833Hypometric upward saccades1MME CL E G H4311497764ORPHA13427154120520
HP:0000571HP:0031833Hypometric upward saccades1MME CL E G H4311497764ORPHA11967154120520
HP:0000571HP:0007975Hypometric horizontal saccades1MME CL E G H4311497764ORPHA13427154120520
HP:0000571HP:0007975Hypometric horizontal saccades1MME CL E G H4311497764ORPHA11967154120520
HP:0000571HP:0007975Hypometric horizontal saccades1MRE11 CL E G H4361604391Ataxia-telangiectasia-like disorder 1604391C1858391OMIM112597230600814
HP:0000571HP:0007975Hypometric horizontal saccades1MRE11 CL E G H4361604391Ataxia-telangiectasia-like disorder 1604391C1858391OMIM112587230600814
HP:0000571HP:0031833Hypometric upward saccades1MRE11 CL E G H4361604391Ataxia-telangiectasia-like disorder 1604391C1858391OMIM112597230600814
HP:0000571HP:0031833Hypometric upward saccades1MRE11 CL E G H4361604391Ataxia-telangiectasia-like disorder 1604391C1858391OMIM112587230600814
HP:0000571HP:0007975Hypometric horizontal saccades1NKX6-2 CL E G H84504527497ORPHA115119321605955
HP:0000571HP:0007975Hypometric horizontal saccades1NKX6-2 CL E G H84504527497ORPHA111919321605955
HP:0000571HP:0031833Hypometric upward saccades1NKX6-2 CL E G H84504527497ORPHA115119321605955
HP:0000571HP:0031833Hypometric upward saccades1NKX6-2 CL E G H84504527497ORPHA111919321605955
HP:0000571HP:0031833Hypometric upward saccades1NKX6-2 CL E G H84504617560SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY617560C4479653OMIM115119321605955
HP:0000571HP:0031833Hypometric upward saccades1NKX6-2 CL E G H84504617560SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY617560C4479653OMIM111919321605955
HP:0000571HP:0007975Hypometric horizontal saccades1NKX6-2 CL E G H84504617560SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY617560C4479653OMIM115119321605955
HP:0000571HP:0007975Hypometric horizontal saccades1NKX6-2 CL E G H84504617560SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY617560C4479653OMIM111919321605955
HP:0000571HP:0031833Hypometric upward saccades1NPHP1 CL E G H4867609583Joubert syndrome 4609583C1846790OMIM16267905607100
HP:0000571HP:0031833Hypometric upward saccades1NPHP1 CL E G H4867609583Joubert syndrome 4609583C1846790OMIM15327905607100
HP:0000571HP:0007975Hypometric horizontal saccades1NPHP1 CL E G H4867609583Joubert syndrome 4609583C1846790OMIM16267905607100
HP:0000571HP:0007975Hypometric horizontal saccades1NPHP1 CL E G H4867609583Joubert syndrome 4609583C1846790OMIM15327905607100
HP:0000571HP:0007975Hypometric horizontal saccades1PLA2G6 CL E G H8398199351ORPHA15139039603604
HP:0000571HP:0007975Hypometric horizontal saccades1PLA2G6 CL E G H8398199351ORPHA14319039603604
HP:0000571HP:0031833Hypometric upward saccades1PLA2G6 CL E G H8398199351ORPHA15139039603604
HP:0000571HP:0031833Hypometric upward saccades1PLA2G6 CL E G H8398199351ORPHA14319039603604
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0000571HP:0000571Hypometric saccades0CACNA1G CL E G H8913458803ORPHA03741394604065
HP:0000571HP:0000571Hypometric saccades0CACNA1G CL E G H8913458803ORPHA03571394604065
HP:0000571HP:0000571Hypometric saccades0DNAJC6 CL E G H9829615528Parkinson disease 19a, juvenile-onset615528C3809811OMIM021515469608375
HP:0000571HP:0000571Hypometric saccades0DNAJC6 CL E G H9829615528Parkinson disease 19a, juvenile-onset615528C3809811OMIM017315469608375
HP:0000571HP:0000571Hypometric saccades0MME CL E G H4311617018Spinocerebellar ataxia 43617018C4310763OMIM03427154120520
HP:0000571HP:0000571Hypometric saccades0MME CL E G H4311617018Spinocerebellar ataxia 43617018C4310763OMIM01967154120520
HP:0000571HP:0000571Hypometric saccades0SLC1A3 CL E G H6507612656Episodic ataxia, type 6612656C2675211OMIM018510941600111
HP:0000571HP:0000571Hypometric saccades0SLC1A3 CL E G H6507612656Episodic ataxia, type 6612656C2675211OMIM017610941600111
HP:0000571HP:0000571Hypometric saccades0SPTBN2 CL E G H6712615386Spinocerebellar ataxia, autosomal recessive 14615386C3809327OMIM056911276604985
HP:0000571HP:0000571Hypometric saccades0SPTBN2 CL E G H6712615386Spinocerebellar ataxia, autosomal recessive 14615386C3809327OMIM047811276604985
HP:0000571HP:0007975Hypometric horizontal saccades1CACNA1G CL E G H8913458803ORPHA03741394604065
HP:0000571HP:0007975Hypometric horizontal saccades1CACNA1G CL E G H8913458803ORPHA03571394604065
HP:0000571HP:0031833Hypometric upward saccades1CACNA1G CL E G H8913458803ORPHA03741394604065
HP:0000571HP:0031833Hypometric upward saccades1CACNA1G CL E G H8913458803ORPHA03571394604065
HP:0000571HP:0031833Hypometric upward saccades1DNAJC6 CL E G H9829615528Parkinson disease 19a, juvenile-onset615528C3809811OMIM021515469608375
HP:0000571HP:0031833Hypometric upward saccades1DNAJC6 CL E G H9829615528Parkinson disease 19a, juvenile-onset615528C3809811OMIM017315469608375
HP:0000571HP:0007975Hypometric horizontal saccades1DNAJC6 CL E G H9829615528Parkinson disease 19a, juvenile-onset615528C3809811OMIM021515469608375
HP:0000571HP:0007975Hypometric horizontal saccades1DNAJC6 CL E G H9829615528Parkinson disease 19a, juvenile-onset615528C3809811OMIM017315469608375
HP:0000571HP:0007975Hypometric horizontal saccades1MME CL E G H4311617018Spinocerebellar ataxia 43617018C4310763OMIM03427154120520
HP:0000571HP:0007975Hypometric horizontal saccades1MME CL E G H4311617018Spinocerebellar ataxia 43617018C4310763OMIM01967154120520
HP:0000571HP:0031833Hypometric upward saccades1MME CL E G H4311617018Spinocerebellar ataxia 43617018C4310763OMIM03427154120520
HP:0000571HP:0031833Hypometric upward saccades1MME CL E G H4311617018Spinocerebellar ataxia 43617018C4310763OMIM01967154120520
HP:0000571HP:0007975Hypometric horizontal saccades1SLC1A3 CL E G H6507612656Episodic ataxia, type 6612656C2675211OMIM018510941600111
HP:0000571HP:0007975Hypometric horizontal saccades1SLC1A3 CL E G H6507612656Episodic ataxia, type 6612656C2675211OMIM017610941600111
HP:0000571HP:0031833Hypometric upward saccades1SLC1A3 CL E G H6507612656Episodic ataxia, type 6612656C2675211OMIM018510941600111
HP:0000571HP:0031833Hypometric upward saccades1SLC1A3 CL E G H6507612656Episodic ataxia, type 6612656C2675211OMIM017610941600111
HP:0000571HP:0007975Hypometric horizontal saccades1SPTBN2 CL E G H6712615386Spinocerebellar ataxia, autosomal recessive 14615386C3809327OMIM056911276604985
HP:0000571HP:0007975Hypometric horizontal saccades1SPTBN2 CL E G H6712615386Spinocerebellar ataxia, autosomal recessive 14615386C3809327OMIM047811276604985
HP:0000571HP:0031833Hypometric upward saccades1SPTBN2 CL E G H6712615386Spinocerebellar ataxia, autosomal recessive 14615386C3809327OMIM056911276604985
HP:0000571HP:0031833Hypometric upward saccades1SPTBN2 CL E G H6712615386Spinocerebellar ataxia, autosomal recessive 14615386C3809327OMIM047811276604985


Genes (12) :APTX CACNA1G DNAJC6 GBA GRM1 MME MRE11 NKX6-2 NPHP1 PLA2G6 SLC1A3 SPTBN2

Diseases (15) :208920 458803 615528 324262 614831 497764 617018 604391 527497 617560 609583 199351 612656 615386 231005
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.