Horizontal nystagmus

Symptom Information:

Symptom ID: HPO:0000666
Synonyms:
Nystagmus, horizontal [HPO:0000666]
Horizontal nystagmus [OMIM:Horizontal nystagmus]
Nystagmus, horizontal [OMIM:Nystagmus, horizontal]
Horizontal nystagmus (5%) [OMIM:Horizontal nystagmus (5%)]
Horizontal nystagmus (about half of patients) [OMIM:Horizontal nystagmus (about half of patients)]
Horizontal nystagmus (in 1 patient) [OMIM:Horizontal nystagmus (in 1 patient)]
Nystagmus, horizontal (rare) [OMIM:Nystagmus, horizontal (rare)]
Quality:
Cross references:
OMIM: "Horizontal nystagmus" [OMIM:Horizontal nystagmus]
OMIM: "Nystagmus, horizontal" [OMIM:Nystagmus, horizontal]
OMIM: "Horizontal nystagmus (5%)" [OMIM:Horizontal nystagmus (5%)]
OMIM: "Horizontal nystagmus (about half of patients)" [OMIM:Horizontal nystagmus (about half of patients)]
OMIM: "Horizontal nystagmus (in 1 patient)" [OMIM:Horizontal nystagmus (in 1 patient)]
OMIM: "Nystagmus, horizontal (rare)" [OMIM:Nystagmus, horizontal (rare)]
Is a (Direct Parents):
HPO         Nystagmus
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye physiology(HPO:0012373)
             Abnormality of eye movement(HPO:0000496)
                Abnormal involuntary eye movements(HPO:0012547)
                   Nystagmus(HPO:0000639)
                      Horizontal nystagmus(HPO:0000666)
MedDRA:
Database Frequency: 32 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
ALG13-CDG (Orphanet:324422)
Alström syndrome (Orphanet:64)
Autosomal dominant microcephaly (Orphanet:2514)
Autosomal dominant optic atrophy and congenital deafness (Orphanet:3212)
Autosomal dominant optic atrophy, classic type (Orphanet:98673)
Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome (Orphanet:363429)
Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency (Orphanet:324262)
Autosomal recessive optic atrophy, OPA7 type (Orphanet:227976)
Autosomal recessive spastic ataxia with leukoencephalopathy (Orphanet:314603)
CEREBRAL PALSY, ATAXIC, AUTOSOMAL RECESSIVE (OMIM:605388)
Cone dystrophy with supernormal rod response (Orphanet:209932)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Gaucher disease - ophthalmoplegia - cardiovascular calcification (Orphanet:2072)
LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM (OMIM:614381)
LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA (OMIM:608809)
Lethal encephalopathy due to mitochondrial and peroxisomal fission defect (Orphanet:330050)
Leukoencephalopathy - metaphyseal chondrodysplasia (Orphanet:83629)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6 (OMIM:608840)
NYSTAGMUS 1, CONGENITAL, X-LINKED (OMIM:310700)
NYSTAGMUS 2, CONGENITAL, AUTOSOMAL DOMINANT (OMIM:164100)
NYSTAGMUS 6, CONGENITAL, X-LINKED (OMIM:300814)
OPTIC ATROPHY 1 (OMIM:165500)
OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY (OMIM:212550)
PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION (OMIM:172500)
PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM (OMIM:614501)
Perrault Syndrome 5 (OMIM:616138)
Rolandic epilepsy - paroxysmal exercise-induced dystonia - writer's cramp (Orphanet:163727)
SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE (OMIM:611302)
USHER SYNDROME, TYPE IIIB (OMIM:614504)
WERNICKE-KORSAKOFF SYNDROME (OMIM:277730)
Wolfram syndrome 1 (OMIM:222300)