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Death Statistics for Types of Coordination and balance conditions

Deaths and Coordination and balance conditions:

This section presents information about the death rate statistics for the various types of Coordination and balance conditions.

Death Statistics for Types of Coordination and balance conditions

Disease

Death Rate Estimate

US deaths estimate

Statistic Used for Calculation

Spinocerebellar ataxia, autosomal recessive 6 N/A N/A No information
Spinocerebellar ataxia 18 N/A N/A No information
Spinocerebellar ataxia 27 N/A N/A No information
Spinocerebellar ataxia 19 N/A N/A No information
Spinocerebellar ataxia 28 N/A N/A No information
Spinocerebellar ataxia 29 N/A N/A No information
Spinocerebellar ataxia, autosomal dominant N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 4 N/A N/A No information
Spinocerebellar ataxia 16 N/A N/A No information
Spinocerebellar ataxia 25 N/A N/A No information
Spinocerebellar ataxia 11 N/A N/A No information
Spinocerebellar ataxia 20 N/A N/A No information
Spinocerebellar ataxia 12 N/A N/A No information
Spinocerebellar ataxia 21 N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 1 N/A N/A No information
Spinocerebellar ataxia 13 N/A N/A No information
Spinocerebellar ataxia 22 N/A N/A No information
Spinocerebellar ataxia 14 N/A N/A No information
Spinocerebellar ataxia 23 N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 3 N/A N/A No information
Spinocerebellar ataxia 15 N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 5 N/A N/A No information
Spinocerebellar ataxia 17 N/A N/A No information
Spinocerebellar ataxia 26 N/A N/A No information
Balance disorders N/A N/A No information
Spinocerebellar ataxia 2 N/A N/A No information
Spinocerebellar ataxia 4 N/A N/A No information
Spinocerebellar ataxia 5 N/A N/A No information
Spinocerebellar ataxia, Machado-Joseph type I N/A N/A No information
Parkinson's disease dementia, familial N/A N/A No information
Primary Parkinsonism N/A N/A No information
Genetic Parkinson disease N/A N/A No information
Parkinson disease, genetic types N/A N/A No information
Parkinson disease 4, autosomal dominant, Lewy body N/A N/A No information
Parkinson disease 7, autosomal recessive, early-onset N/A N/A No information
Spinocerebellar ataxia, X-linked, 2 N/A N/A No information
Spinocerebellar ataxia, X-linked, 3 N/A N/A No information
Parkinson disease 7, autosomal recessive early-onset (PARK7) N/A N/A No information
Parkinson disease 4, autosomal dominant Lewy body (PARK4) N/A N/A No information
Parkinson disease 11 (PARK11) N/A N/A No information
Parkinson disease 13 (PARK13) N/A N/A No information
Parkinson disease 5 (PARK5) N/A N/A No information
Parkinson disease 9 (PARK9) N/A N/A No information
Idiopathic Parkinson's disease N/A N/A No information
Parkinson disease, familial, type 1 (PARK1) N/A N/A No information
Parkinson disease 6, autosomal recessive early-onset (PARK6) N/A N/A No information
Parkinson disease 2, autosomal recessive juvenile (PARK2) N/A N/A No information
Parkinson disease 10 (PARK10) N/A N/A No information
Parkinson disease 12 (PARK12) N/A N/A No information
Parkinson disease 8 (PARK8) N/A N/A No information
Parkinson disease 3, autosomal dominant Lewy body (PARK3) N/A N/A No information
Mitochondrial Parkinson's disease N/A N/A No information
Parkinson's Disease approx 1 in 272 or 0.37% or 1 million people in USA 1 million people (unreliable estimate) 1 million people (unreliable estimate)
Multiple Sclerosis, Susceptibility To, 1 N/A N/A No information
Multiple Sclerosis, Susceptibility To, 2 N/A N/A No information
Multiple Sclerosis, Susceptibility To, 3 N/A N/A No information
Multiple Sclerosis, Susceptibility To, 4 N/A N/A No information
Joubert Syndrome 10 N/A N/A No information
Joubert Syndrome 9 N/A N/A No information
Joubert Syndrome 8 N/A N/A No information
Joubert Syndrome 7 N/A N/A No information
Joubert Syndrome 6 N/A N/A No information
Joubert Syndrome 5 N/A N/A No information
Joubert Syndrome 4 N/A N/A No information
Joubert Syndrome 3 N/A N/A No information
Joubert Syndrome 2 N/A N/A No information
Joubert Syndrome 1 N/A N/A No information
Benign Multiple Sclerosis N/A N/A No information
Relapsing/remitting multiple sclerosis N/A N/A No information
Secondary chronic progressive multiple sclerosis N/A N/A No information
Primary progressive multiple sclerosis N/A N/A No information
Marburg multiple sclerosis N/A N/A No information
Optic-spinal form of multiple sclerosis N/A N/A No information
Balo disease N/A N/A No information
Multiple Sclerosis N/A N/A 1-in-700 (NIAID)
Astasis N/A N/A No information
Vestibular seizure N/A N/A No information
Alcoholic cerebellar degeneration N/A N/A No information
Optic ataxia N/A N/A No information
Festinating gait N/A N/A No information
Spastic gait N/A N/A No information
Myopathic gait N/A N/A No information
Scissor gait N/A N/A No information
Sensory ataxia N/A N/A No information
Antalgic gait N/A N/A No information
Magnetic gait N/A N/A No information
Steepage gait N/A N/A No information
Continous dizziness similar to Menier'e disease N/A N/A No information
Titubation N/A N/A No information
Alcohol drinking N/A N/A No information
Alcoholic intoxication N/A N/A No information
Alcohol-Induced Disorders N/A N/A No information
Charcot-Marie-Tooth disease with ptosis and parkinsonism N/A N/A No information
Parkinsonism, early onset with mental retardation N/A N/A No information
Amyotrophic lateral sclerosis-parkinsonism/dementia complex 2 N/A N/A No information
Amyotrophic lateral sclerosis-parkinsonism-dementia complex N/A N/A No information
Infantile parkinsonism N/A N/A No information
Spinocerebellar ataxia 3 N/A N/A No information
Parkinson disease, juvenile, autosomal recessive N/A N/A No information
Parkinson disease, familial, Type 1 N/A N/A No information
Parkinson disease 12 N/A N/A No information
Parkinson disease 13 N/A N/A No information
Parkinsonism, early-onset -- mental retardation N/A N/A No information
Parkinson disease 3 N/A N/A No information
Parkinson disease 9 N/A N/A No information
Parkinson disease 8 N/A N/A No information
Parkinson disease 6, autosomal recessive, recessive early-onset N/A N/A No information
Parkinson disease 10 N/A N/A No information
Parkinson disease 11 N/A N/A No information
Sea sickness N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 2 N/A N/A No information
Aniridia cerebellar ataxia mental deficiency N/A N/A No information
Vestibular neuritis N/A N/A No information
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy N/A N/A No information
Deafness hyperuricemia neurologic ataxia N/A N/A No information
Deafness mixed with perilymphatic Gusher, X-linked N/A N/A No information
Ataxia-oculomotor apraxia syndrome N/A N/A No information
Ataxia-deafness syndrome N/A N/A No information
Ataxia, Hereditary, Autosomal Dominant N/A N/A No information
Ataxia spastic congenital miosis N/A N/A No information
Ataxia tapetoretinal degeneration N/A N/A No information
Ataxia with Vitamin E Deficiency N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 7 N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 9 N/A N/A No information
Ataxia, spastic, 3, autosomal recessive N/A N/A No information
Fronto-temporal dementia and Parkinsonism linked to chromosome 17 (FTDP-17) N/A N/A No information
Spinocerebellar ataxia 8 N/A N/A No information
Spinocerebellar ataxia, X-linked, 5 N/A N/A No information
Spinocerebellar ataxia -- dysmorphism N/A N/A No information
Spinocerebellar ataxia with axonal neuropathy, type 2 N/A N/A No information
Spinocerebellar ataxia, X-linked, type 4 N/A N/A No information
Spinocerebellar Ataxia 9 N/A N/A No information
Friedreich's ataxia N/A N/A No information
Spinocerebellar Ataxia N/A N/A No information
Friedreich ataxia N/A N/A estimated 1 per 40,000 people are affected by Friedreich ataxia, Genetics Home Reference website
Cerebral Palsy, Ataxic, Autosomal Recessive N/A N/A No information
Romberg's sign N/A N/A No information
Infantile onset spinocerebellar ataxia N/A N/A No information
Spinocerebellar ataxia, X-linked, 4 N/A N/A No information
Spinocerebellar ataxia, Machado-Joseph type IV N/A N/A No information
Spinocerebellar degenerescence, book type N/A N/A No information
Spinocerebellar ataxia, Machado-Joseph type III N/A N/A No information
Spinocerebellar ataxia 10 N/A N/A No information
Spinocerebellar ataxia, Machado-Joseph type II N/A N/A No information
Spinocerebellar ataxia, Machado-Joseph type V N/A N/A No information
Spinocerebellar ataxia -- amyotrophy -- deafness N/A N/A No information
Spinocerebellar ataxia-dysmorphism syndrome N/A N/A No information
Marinesco-Sjogren syndrome N/A N/A No information
Marinesco-Sjogren I N/A N/A No information
Chylomicron retention disease with Marinesco-Sjogren syndrome N/A N/A No information
Marinesco-Sjogren-like syndrome (MSLS) N/A N/A No information
Dystonia-Parkinsonism, Adult-Onset N/A N/A No information
Neuropathy -- ataxia -- retinitis pigmentosa N/A N/A No information
Neuropathy ataxia and retinis pigmentosa N/A N/A No information
Ataxia N/A N/A No information
Bird-headed dwarfism with progressive ataxia, Insulin-resistant diabetes, goiter and primary gonadal insufficiency N/A N/A No information
Renal tubulopathy -- diabetes mellitus -- cerebellar ataxia N/A N/A No information
Ataxia -- diabetes -- goiter -- gonadal insufficiency N/A N/A No information
Ataxia Telangiectasia N/A N/A 1 per 40,000 - 100,000 people worldwide suffer from ataxia-telangiectasia, Genetics Home Reference website
Episodic ataxia, type 7 N/A N/A No information
Episodic ataxia syndrome N/A N/A No information
Episodic ataxia, type 1 N/A N/A No information
Episodic ataxia, type 2 N/A N/A No information
Episodic ataxia, type 3 N/A N/A No information
Episodic ataxia, type 4 N/A N/A No information
Episodic ataxia, type 5 N/A N/A No information
Episodic ataxia, type 6 N/A N/A No information
Ataxia -- hypogonadism -- choroidal dystrophy N/A N/A No information
Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance N/A N/A No information
Friedreich ataxia -- congenital glaucoma N/A N/A No information
Ataxia, spastic with congenital miosis N/A N/A No information
Ataxia with fasciculations N/A N/A No information
Angelman syndrome N/A N/A 1 per 12,000 - 20,000 people are affected by Angelman syndrome, Genetics Home Reference website
Prader-Willi syndrome N/A N/A estimated 1 per 10,000 - 25,000 people suffer from Prader-Willi syndrome, Genetics Home Reference website
Brachydactyly nystagmus cerebellar ataxia N/A N/A No information
Huntington's Disease N/A N/A estimated 3-7 per 100,000 people of European ancestry suffer from Huntington disease, Genetics Home Reference website
Machado-Joseph Disease N/A N/A rare
Dentatorubral Pallidoluysian Atrophy N/A N/A No information
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem response N/A N/A No information
Cerebellar ataxia, infantile with progressive external ophthalmoplegia N/A N/A No information
ARCA N/A N/A No information
Hypobetalipoproteinaemia -- ataxia -- hearing loss N/A N/A No information
Gluten ataxia N/A N/A No information
Cerebellar ataxia, autosomal recessive N/A N/A No information
Cerebellar ataxia type 1, autosomal recessive N/A N/A No information
Cerebellar ataxia, X-linked N/A N/A No information
Cerebellar ataxia, dominant pure N/A N/A No information
Anaemia, sideroblastic, X-linked -- ataxia N/A N/A No information
Cerebellar hypoplasia N/A N/A No information
Cerebellar ataxia -- ectodermal dysplasia N/A N/A No information
Cerebellar ataxia -- areflexia -- pes cavus -- optic atrophy -- sensorineural hearing loss N/A N/A No information
Cerebellar ataxia -- intellectual deficit -- optic atrophy -- skin abnormalities N/A N/A No information
Cerebellar Ataxia, Deafness and Narcolepsy N/A N/A No information
Cerebellar ataxia syndrome N/A N/A No information
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss N/A N/A No information
Cerebellar hypoplasia -- endosteal sclerosis N/A N/A No information
Cerebellar parenchymal degeneration N/A N/A No information
Hereditary non-progressive cerebellar ataxia syndrome of early onset N/A N/A No information
Early-onset non-progressive cerebellar ataxia syndrome, dominantly inherited N/A N/A No information
Hereditary cerebellar ataxia syndrome of early onset N/A N/A No information
Cerebellar vermis hypoplasia -- oligophrenia -- congenital ataxia -- coloboma -- hepatic fibrosis N/A N/A No information
Anemia, sideroblastic spinocerebellar ataxia N/A N/A No information
Myelocerebellar disorder N/A N/A No information
Myoclonus, cerebellar ataxia, deafness N/A N/A No information
Leukodystrophy with oligodontia N/A N/A No information
Hereditary ataxia N/A N/A No information
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa and Cataract N/A N/A No information
East Syndrome N/A N/A No information
Disseminated Sclerosis with Narcolepsy N/A N/A No information
Hereditary paroxysmal cerebral ataxia N/A N/A No information
Unverricht-Lundborg disease N/A N/A No information
Unverricht-Lundborg syndrome N/A N/A No information
Ataxia, episodic -- vertigo -- tinnitus -- myokymia N/A N/A No information
Lundberg I N/A N/A No information
Benign Paroxysmal Positional Vertigo N/A N/A No information
Ménière's disease N/A N/A about 10,000 people in Australia
Vertigo N/A N/A No information
Vestibular neuronitis N/A N/A No information
Perilymph fistula N/A N/A No information
Perilymphatic fistula N/A N/A No information
Giant axonal neuropathy N/A N/A No information
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis N/A N/A No information
Cataract -- ataxia -- deafness N/A N/A No information
Ataxia -- oculomotor apraxia, type 1 N/A N/A No information
Vertigo, benign paroxysmal, in childhood N/A N/A No information
Joubert Syndrome N/A N/A rare
Miller Fisher Syndrome N/A N/A rare
Cerebelloparenchymal autosomal recessive disorder 3 N/A N/A No information
Cerebelloparenchymal disorder 3 N/A N/A No information
Familial dysautonomia N/A N/A No information
Labyrinthitis syndrome N/A N/A No information
Multiple sclerosis -- ichthyosis -- factor 8 deficiency N/A N/A No information
Myoclonus-ataxia N/A N/A No information
Dykes-Markes-Harper syndrome N/A N/A No information
Arachnodactyly -- ataxia -- cataract -- aminoaciduria -- mental retardation N/A N/A No information
Quadrupedal gait, primitive speech and severe mental retardation N/A N/A No information
Opthalmoplegia ataxia hypoacusis N/A N/A No information
Vestibulocochlear Nerve Diseases N/A N/A No information
Vestibulocochlear dysfunction progressive familial N/A N/A No information
Enlarged vestibular aqueduct syndrome N/A N/A No information
Vestibulocochlear dysfunction progressive familial type N/A N/A No information
Williams Syndrome N/A N/A estimated 1 per 7,500 - 20,000 people suffer from Williams syndrome, Genetics Home Reference website
MASA Syndrome N/A N/A No information
Ophtalmoplegia -- ataxia -- hypoacusis N/A N/A No information
Aniridia ataxia renal agenesis psychomotor retardation N/A N/A No information
Borud Syndrome N/A N/A No information
Cutler Syndrome N/A N/A No information
Jequier-Deonna Syndrome N/A N/A No information
Robinson syndrome N/A N/A No information
Mann syndrome N/A N/A No information
May-White syndrome N/A N/A No information
CACH syndrome N/A N/A No information
Baughman syndrome N/A N/A No information
Combarros Calleja Leno syndrome N/A N/A No information
Mal de debarquement N/A N/A No information
CANOMAD syndrome N/A N/A No information
Conorenal Syndrome N/A N/A No information
Fanconi-Turler syndrome N/A N/A No information
Gerlier disease N/A N/A No information
Reardon-Wilson-Cavanagh syndrome N/A N/A No information
ARTS syndrome N/A N/A No information
Richards-Rundle syndrome N/A N/A No information
Mousa-Al Din-Al Nassar syndrome N/A N/A No information
Megalencephalic leukoencephalopathy with subcortical cysts N/A N/A No information
Dysequilibrium syndrome N/A N/A No information
Harding ataxia N/A N/A No information
Luteinizing hormone releasing hormone, deficiency of, with ataxia N/A N/A No information
COACH syndrome N/A N/A No information
Posterior column ataxia with retinitis pigmentosa N/A N/A No information
Furukawa-Takagi-Nakao syndrome N/A N/A No information
Spastic ataxia, Charlevoix-Saguenay type N/A N/A No information
Schroer-Hammer-Mauldin syndrome N/A N/A No information
Telfer-Sugar-Jaeger syndrome N/A N/A No information
Sylvester (P.E.) syndrome N/A N/A No information
Bhaskar-Jagannathan syndrome N/A N/A No information
Bangstad syndrome N/A N/A No information
Fenton-Wilkinson-Toselano syndrome N/A N/A No information
Jeune-Tommasi syndrome N/A N/A No information
Boucher-Neuhauser syndrome N/A N/A No information
Erythrokeratodermia ataxia N/A N/A No information
Marie type ataxia N/A N/A No information
Erythrokeratodermia with ataxia N/A N/A No information
Westphal-Leyden ataxia N/A N/A No information

Types of Coordination and balance conditions

For more information about types of Coordination and balance conditions, refer to our section on types of Coordination and balance conditions. See also more information on death information for Coordination and balance conditions.

 

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