Tremor, Hereditary Essential, 4,Leukemia, Chronic Myeloid,Hepatitis A,Semantic Dementia,Deficiency Anemia,Frontotemporal Dementia

Skin Squamous Cell Carcinoma,Cone-Rod Dystrophy 2,Meningioma, Familial

Diamond-Blackfan Anemia,Hermansky-Pudlak Syndrome 3

Pediatric Meningioma,Temporal Lobe Neoplasm,Diffuse Astrocytoma,Mixed Glioma,Oligodendroglioma,Childhood Oligodendroglioma,Adult Oligodendroglioma,Hand, Foot And Mouth Disease,Mouth Disease,Brain Glioma

Spinal Muscular Atrophy

Paraneoplastic Polyneuropathy,Fragile X Syndrome,Neurodevelopmental Disorder With Or Without Autistic Features And/Or Structural Brain Abnormalities

Learning Disability,Chromosomal Disease,Echolalia,Mutism,Retinitis Pigmentosa,Migraine With Or Without Aura 1,Fibromyalgia,Kagami-Ogata Syndrome,Tremor,Speech Disorder,Cataract 24,Phobia, Specific,Myotonic Disease,Gene Duplication Disease,Amyotrophic Lateral Sclerosis 1,Myotonic Dystrophy 1,Angelman Syndrome,Middle Cranial Fossa Meningioma,Intestinal Disaccharidase Deficiency,Muscular Dystrophy,Movement Disease,Spinocerebellar Ataxia 8,Myoclonic Cerebellar Dyssynergia,Essential Tremor,Influenza,Fmr1 Disorders,Spinocerebellar Ataxia 1,Dementia,Cerebellar Disease,Childhood Disintegrative Disease,Parkinson Disease, Late-Onset,Patella, Chondromalacia Of,Premature Menopause,Amenorrhea,Speech And Communication Disorders,Phobic Disorder,Myotonic Dystrophy 2,Chromosome 14q11-Q22 Deletion Syndrome,Schizoid Personality Disorder,Sotos Syndrome 1,Ovarian Disease,Alacrima, Achalasia, And Mental Retardation Syndrome,Autosomal Dominant Cerebellar Ataxia,Benign Epilepsy With Centrotemporal Spikes,Spinocerebellar Ataxia 10,Prader-Willi Syndrome,Social Phobia,Friedreich Ataxia,Turner Syndrome,Disease Of Mental Health,Lubs X-Linked Mental Retardation Syndrome,Dentatorubral-Pallidoluysian Atrophy,Meier-Gorlin Syndrome 2,Mental Retardation, X-Linked, With Cerebellar Hypoplasia And Distinctive Facial Appearance,Fragile X Tremor/Ataxia Syndrome,Fragile X Syndrome,Schizophrenia,Beckwith-Wiedemann Syndrome,Restless Legs Syndrome,Chromosome Xq27.3-Q28 Duplication Syndrome,Phelan-Mcdermid Syndrome,Digeorge Syndrome,X-Linked Monogenic Disease,Huntington Disease-Like 2,Kaufman Oculocerebrofacial Syndrome,Non-Syndromic X-Linked Intellectual Disability,Spinocerebellar Ataxia, X-Linked 3,Spinocerebellar Ataxia, X-Linked 4,Velocardiofacial Syndrome,Huntington Disease,Attention Deficit-Hyperactivity Disorder,Fragile X-Associated Tremor/Ataxia Syndrome,Williams-Beuren Syndrome,X-Linked Hereditary Ataxia,Specific Developmental Disorder,Pervasive Developmental Disorder,Autism Spectrum Disorder,Atypical Autism,Multiple System Atrophy 1,Epilepsy, Idiopathic Generalized 9,Mucopolysaccharidosis, Type Ii,Anxiety,Premature Ovarian Failure 1,Chromosomal Deletion Syndrome,Chromosomal Duplication Syndrome,Spinal And Bulbar Muscular Atrophy, X-Linked 1,Autism

Epilepsy, Idiopathic Generalized 5,Chromosome 2q37 Deletion Syndrome

Gait Apraxia,Low-Grade Astrocytoma,Paraneoplastic Polyneuropathy,Breast Cancer,Partial Fetal Alcohol Syndrome,Lung Cancer