nystagmus
Basic Information
- Identifier
- SYMP_0000338
- Notation
- SYMP:0000338
- Category
- symptoms
- Synonyms
-
- rapid involuntary rhythmic eye movement
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- Leber congenital amaurosis 17
- Leber congenital amaurosis 3
- Leber congenital amaurosis 5
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- autosomal recessive spinocerebellar ataxia 18
- autosomal recessive spinocerebellar ataxia 2
- autosomal recessive spinocerebellar ataxia 22
- autosomal recessive spinocerebellar ataxia 31
- autosomal recessive spinocerebellar ataxia 33
- autosomal recessive spinocerebellar ataxia 8
- bilateral optic nerve hypoplasia
- blue cone monochromacy
- central nervous system immature teratoma
- cerebellar ataxia type 43
- cerebellar ataxia type 47
- cerebellar atrophy, visual impairment, and psychomotor retardation
- cerebellar hyplasia/atrophy, epilepsy, and global developmental delay
- cerebral degeneration
- chromosome 2q31.1 duplication syndrome
- combined oxidative phosphorylation deficiency 36
- combined oxidative phosphorylation deficiency 43
- combined oxidative phosphorylation deficiency 7
- complex cortical dysplasia with other brain malformations 6
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- congenital stationary night blindness 1C
- congenital stationary night blindness 1E
- congenital stationary night blindness 1F
- congenital stationary night blindness 1G
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- hypomyelinating leukodystrophy 16
- infantile hypotonia with psychomotor retardation and characteristic facies-3
- internuclear ophthalmoplegia
- labyrinthitis
- mitochondrial DNA depletion syndrome 17
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- mitochondrial complex V (ATP synthase) deficiency mitochondrial type 1
- mitochondrial complex V (ATP synthase) deficiency nuclear type 4
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- mitochondrial complex V (ATP synthase) deficiency nuclear type 4B
- mitochondrial complex V (ATP synthase) deficiency nuclear type 6
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- obsolete Haemophilus influenzae meningitis
- obsolete acute suppurative otitis media with tympanic membrane intact
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- obsolete epidermal nevus
- obsolete glioma of visual pathway
- obsolete labyrinthine disease
- obsolete peripheral dysostosis
- ocular albinism with sensorineural deafness
- ocular motility disease
- oculocutaneous albinism type IA
- oculocutaneous albinism type IB
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- oculocutaneous albinism type VI
- optic nerve neoplasm
- posterior fossa group A ependymoma
- posterior fossa group B ependymoma
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