Horizontal nystagmus
Symptom Information:
Symptom ID: | HPO:0000666 | |||||||
Synonyms: |
|
|||||||
Quality: | ||||||||
Cross references: |
|
|||||||
Is a (Direct Parents): |
|
|||||||
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) |