Refsum Disease, Classic,Agnosia,Spinocerebellar Ataxia Type 1 With Axonal Neuropathy,Pontocerebellar Hypoplasia, Type 7,Spastic Ataxia, Charlevoix-Saguenay Type,Mitochondrial Dna Depletion Syndrome 7,Motor Peripheral Neuropathy,Oculomotor Apraxia,Choreatic Disease,Cerebellar Disease,Tay-Sachs Disease,Ataxia-Oculomotor Apraxia 3,Dystonia,Prostate Squamous Cell Carcinoma,Neuropathy,Peripheral Nervous System Disease,Cardiofaciocutaneous Syndrome 1,Vestibular Nystagmus,Ataxia With Vitamin 3 Deficiency,Autosomal Dominant Cerebellar Ataxia,Xeroderma Pigmentosum, Variant Type,Friedreich Ataxia,Disease Of Mental Health,Achalasia-Addisonianism-Alacrima Syndrome,Multiple Acyl-Coa Dehydrogenase Deficiency,Dentatorubral-Pallidoluysian Atrophy,Mental Retardation, X-Linked, With Cerebellar Hypoplasia And Distinctive Facial Appearance,Spinocerebellar Ataxia 14,Spinocerebellar Ataxia, Autosomal Recessive, With Axonal Neuropathy 2,Coenzyme Q10 Deficiency, Primary, 4,Coenzyme Q10 Deficiency Disease,Lig4 Syndrome,Marinesco-Sjogren Syndrome,Autosomal Recessive Cerebellar Ataxia,Hereditary Ataxia,Spastic Ataxia,Spastic Paraplegia 7, Autosomal Recessive,Coenzyme Q10 Deficiency, Primary, 1,Apraxia,Charcot-Marie-Tooth Disease, Axonal, Type 2cc,Ataxia-Telangiectasia,Ataxia, Early-Onset, With Oculomotor Apraxia And Hypoalbuminemia,Kearns-Sayre Syndrome,Ocular Motor Apraxia

Spinal Muscular Atrophy,Muscular Atrophy,Non-Syndromic X-Linked Intellectual Disability,Al-Raqad Syndrome,Syndromic Intellectual Disability,Autosomal Recessive Non-Syndromic Intellectual Disability,Spinal Muscular Atrophy, Type I