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

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

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

Tremor, Hereditary Essential, 4,Burkitt Lymphoma,Deafness, Autosomal Recessive 17,Aceruloplasminemia

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

Diamond-Blackfan Anemia,Hermansky-Pudlak Syndrome 3

Hemophagocytic Lymphohistiocytosis, Familial, 1,Hemophagocytic Lymphohistiocytosis, Familial, 2,Meckel Diverticulum

Stomatitis,Melanomatosis,Neurodevelopmental Disorder-Craniofacial Dysmorphism-Cardiac Defect-Skeletal Anomalies Syndrome Due To 9q21.3 Microdeletion,Aplastic Anemia,Breast Cancer,Colorectal Cancer,Alacrima, Achalasia, And Mental Retardation Syndrome,Spinocerebellar Ataxia 10,Disease Of Mental Health,Fragile X Syndrome,Mouth Disease,Au-Kline Syndrome,Ptosis

Protoplasmic Astrocytoma,Smallpox

Myopathy,Mixed Cell Uveal Melanoma,Cervical Non-Keratinizing Squamous Cell Carcinoma,Multiminicore Disease,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Fragile X Syndrome,X-Linked Monogenic Disease,Fragile X-Associated Tremor/Ataxia Syndrome,Specific Developmental Disorder,Myopathy, Congenital, With Respiratory Insufficiency And Bone Fractures,Myopathy, Congenital Proximal, With Minicore Lesions,Autism

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

Childhood Absence Epilepsy,Osteopetrosis,Hypophosphatasia,Localized Osteosarcoma,Corneal Dystrophy, Fleck,Hypophosphatasia, Infantile,Hypophosphatasia, Adult,Atrial Septal Defect 2

Spinal Muscular Atrophy

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

Melanoma,Myopathy, Centronuclear, 1,Combined Oxidative Phosphorylation Deficiency 13,Deafness, Autosomal Recessive 70,Nonsyndromic Deafness,Optic Atrophy 3, Autosomal Dominant,Prostate Carcinoma In Situ,Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb,Autosomal Recessive Nonsyndromic Deafness,Aicardi-Goutieres Syndrome,Spastic Ataxia 5,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,2-Aminoadipic 2-Oxoadipic Aciduria,Combined Oxidative Phosphorylation Deficiency,Leigh Syndrome

Epilepsy, Idiopathic Generalized 5,Chromosome 2q37 Deletion Syndrome