|
Abetalipoproteinemia Neuropathy
adult-onset ataxia and polyneuropathy
Ataxia with Fasciculations
Ataxia with Myoclonic Epilepsy and Presenile Dementia
Ataxia, Deafness, and Cardiomyopathy
ATAXIA, INTENTION TREMOR, AND HYPOTONIA SYNDROME, CHILDHOOD-ONSET
ATAXIA, PROGRESSIVE SEIZURES, MENTAL DETERIORATION, AND HEARING LOSS
Ataxia-Microcephaly-Cataract Syndrome
Atonic-Astatic Syndrome of Foerster
Bhaskar Jagannathan Syndrome
Carnitine Acetyltransferase Deficiency
Cataracts, Ataxia, Short Stature, and Mental Retardation
Cerebroretinal Microangiopathy with Calcifications and Cysts +
Chanarin-Dorfman syndrome +
Childhood-onset Neurodegeneration with Ataxia, Tremor, Optic Atrophy, and Cognitive Decline
coenzyme Q10 deficiency disease +
Deafness Hyperuricemia Neurologic Ataxia
Familial Cardiac Lipidosis
familial isolated deficiency of vitamin E
Farber lipogranulomatosis
fragile X-associated tremor/ataxia syndrome
Global Developmental Delay, Progressive Ataxia, and Elevated Glutamine
hypomyelinating leukodystrophy 7
hypotonia, ataxia, and delayed development syndrome
HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME
Hypotonia, Congenital Nystagmus, Ataxia and Abnormal Auditory Brainstem Response
Leukoencephalopathy with Ataxia
lysosomal acid lipase deficiency +
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus
Neurodegeneration with Ataxia and Late-Onset Optic Atrophy
NEURODEVELOPMENTAL DISORDER WITH ATAXIA, HYPOTONIA, AND MICROCEPHALY
neurodevelopmental disorder with eye movement abnormalities and ataxia
Neurodevelopmental Disorder with Impaired Intellectual Development, Hypotonia, and Ataxia
NEURODEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND ATAXIA AND WITH OR WITHOUT SEIZURES
NEURODEVELOPMENTAL DISORDER WITH INTENTION TREMOR, PYRAMIDAL SIGNS, DYSPRAXIA, AND OCULAR ANOMALIES
neuronal ceroid lipofuscinosis +
Neurovisceral Storage Disease with Curvilinear Bodies
OPTIC ATROPHY-ATAXIA-PERIPHERAL NEUROPATHY-GLOBAL DEVELOPMENTAL DELAY SYNDROME
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain
Primary Orthostatic Tremor
progressive myoclonus epilepsy 1B
Reardon Wilson Cavanagh Syndrome
Retinopathy-sensory neuropathy syndrome
Sensory Ataxia, Autosomal Dominant
Sjogren-Larsson syndrome +
Spastic Paraplegia, Ataxia, and Mental Retardation
Spinocerebellar Ataxias +
spondyloepimetaphyseal dysplasia, Genevieve-type
steatotic liver disease +
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
Tapetoretinal Degeneration with Ataxia
Treft Sanborn Carey Syndrome
Tremor of Intention, Ataxia, and Lipofuscinosis
Tryptophanuria with Dwarfism
|
|