This section presents information about the death rate statistics
for the various 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
|
