Viral Infectious Disease,Coronavirus Infectious Disease,Hepatitis E,Middle East Respiratory Syndrome,Avian Influenza,Amyotrophic Lateral Sclerosis 1,Crimean-Congo Hemorrhagic Fever,Noonan Syndrome 1,Influenza,Bacterial Infectious Disease,Japanese Encephalitis,Adult Dermatomyositis,Childhood Type Dermatomyositis,Vaccinia,Immunodeficiency 27b,Immunodeficiency 38 With Basal Ganglia Calcification,Aicardi-Goutieres Syndrome,Vasculopathy, Retinal, With Cerebral Leukoencephalopathy And Systemic Manifestations,Acute Promyelocytic Leukemia,Adams-Oliver Syndrome,Basal Ganglia Calcification,Systemic Lupus Erythematosus,Microphthalmia With Limb Anomalies,Oliver Syndrome

Brain Sarcoma,Angelman Syndrome,Paget'S Disease Of Bone,Xeroderma Pigmentosum, Complementation Group C,Xeroderma Pigmentosum, Variant Type,Xeroderma Pigmentosum, Complementation Group G

Deafness, Autosomal Dominant 69

Rett Syndrome,Primary Hypomagnesemia

Autoinflammation, Panniculitis, And Dermatosis Syndrome,Glycogen Storage Disease Iv,Tooth Agenesis,Incontinentia Pigmenti

Non-Invasive Bladder Papillary Urothelial Neoplasm,Isolated Unilateral Hemispheric Cerebellar Hypoplasia,Periventricular Nodular Heterotopia

Tracheitis,Friedreich Ataxia 2,Cone-Rod Dystrophy 2

Autoimmune Lymphoproliferative Syndrome,Congenital Disorder Of Deglycosylation,Parkinson Disease, Late-Onset,Joubert Syndrome 31,Cleft Palate, Isolated,Brugada Syndrome 9

Progressive Multifocal Leukoencephalopathy,Cleft Lip,Orofacial Cleft 4,Acute Necrotizing Encephalitis,Lip Cancer,Cleft Palate, Isolated,Neuronal Intranuclear Inclusion Disease,Orofacial Cleft 10,Dentatorubral-Pallidoluysian Atrophy,Familial Partial Lipodystrophy,Orofacial Cleft,Tooth Agenesis,Acute Promyelocytic Leukemia,Early-Onset Parkinson'S Disease,Frontotemporal Dementia

Progressive Myoclonus Epilepsy,Supranuclear Palsy, Progressive, 1,Retinitis Pigmentosa,Rem Sleep Behavior Disorder,Lung Cancer Susceptibility 3,Tremor,Optic Nerve Disease,Prion Disease,Gaucher'S Disease,Sphingolipidosis,Alzheimer Disease,Ulnar Nerve Lesion,Radial Nerve Lesion,Amyotrophic Lateral Sclerosis 1,Angelman Syndrome,Motor Neuron Disease,Movement Disease,Neurodegeneration With Brain Iron Accumulation,Testicular Disease,Leber Plus Disease,Essential Tremor,Choreatic Disease,Machado-Joseph Disease,Dementia,Optic Atrophy 1,Cerebellar Disease,Leukoencephalopathy, Hereditary Diffuse, With Spheroids,Parkin Type Of Early-Onset Parkinson Disease,Dystonia,Nervous System Disease,Ovarian Cancer,Charcot-Marie-Tooth Disease,Paratyphoid Fever,Parkinson Disease, Late-Onset,Peripheral Nervous System Disease,Parkinson Disease 3, Autosomal Dominant,Parkinson Disease 1, Autosomal Dominant,Tooth Disease,Pick Disease Of Brain,Postencephalitic Parkinson Disease,Autosomal Dominant Cerebellar Ataxia,Fanconi Anemia, Complementation Group A,Disease Of Mental Health,Gaucher Disease, Type I,Toxic Encephalopathy,Body Mass Index Quantitative Trait Locus 11,Dentatorubral-Pallidoluysian Atrophy,Meier-Gorlin Syndrome 2,Dementia, Lewy Body,Dystonia 12,Schizophrenia,Ophthalmomyiasis,Restless Legs Syndrome,Parkinson Disease 21,Kufor-Rakeb Syndrome,Leprosy 3,Focal Dystonia,Parkinson Disease 10,Attention Deficit-Hyperactivity Disorder,Autism Spectrum Disorder,Multiple System Atrophy 1,Color Agnosia,Leber Hereditary Optic Neuropathy, Modifier Of,Leprosy 2,Mitochondrial Complex I Deficiency, Nuclear Type 1,Epilepsy, Idiopathic Generalized 9,Ptosis,Rett Syndrome,Myoclonic Epilepsy Of Lafora,Autism,Juvenile-Onset Parkinson'S Disease,Early-Onset Parkinson'S Disease,Parkinson Disease 2, Autosomal Recessive Juvenile,Lung Cancer,Parkinson Disease 15, Autosomal Recessive Early-Onset

Amyotrophic Lateral Sclerosis 1,Sarcoma,Osteogenic Sarcoma

Retinitis Pigmentosa,Epilepsy,Middle East Respiratory Syndrome,Alzheimer Disease,Ectodermal Dysplasia,Angelman Syndrome,Luteoma,Cystic Fibrosis,Machado-Joseph Disease,Ethmoid Sinus Adenocarcinoma,Xeroderma Pigmentosum, Complementation Group C,Neuronal Ceroid Lipofuscinosis,Ring Dermoid Of Cornea,Ectodermal Dysplasia 10a, Hypohidrotic/Hair/Nail Type, Autosomal Dominant,Myoclonic Epilepsy Of Lafora,Gordon Holmes Syndrome

Gordon Holmes Syndrome

Familial Renal Papillary Carcinoma,Clear Cell Renal Cell Carcinoma,Dermis Tumor,Familial Isolated Hypoparathyroidism,Leiomyoma Cutis,Retinal Hemangioblastoma,Molluscum Contagiosum,Primary Polycythemia,Pheochromocytoma,Von Hippel-Lindau Syndrome,Renal Cell Carcinoma, Nonpapillary,Cardiovascular Organ Benign Neoplasm,Erythrocytosis, Familial, 2

Cerebellar Ataxia, Deafness, And Narcolepsy, Autosomal Dominant

Chronic Kidney Disease,Crisponi/Cold-Induced Sweating Syndrome 1,Kidney Disease,Hepatocellular Carcinoma

Spasticity,Spastic Ataxia, Charlevoix-Saguenay Type,Fitzsimmons Syndrome,Hereditary Spastic Paraplegia,Rare Ataxia,Complex Hereditary Spastic Paraplegia,Chronic Polyneuropathy,Autosomal Recessive Spastic Ataxia,Cerebellar Disease,Neuropathy,Spinocerebellar Ataxia, Autosomal Recessive 14,Autosomal Dominant Cerebellar Ataxia,Spastic Paraplegia 57, Autosomal Recessive,Dentatorubral-Pallidoluysian Atrophy,Spinocerebellar Ataxia, Autosomal Recessive 8,Spinocerebellar Ataxia, Autosomal Recessive, With Axonal Neuropathy 2,Spastic Ataxia 4,Hereditary Ataxia,Spastic Ataxia,3-Methylglutaconic Aciduria, Type Iii

Congenital Disorder Of Deglycosylation

Amyotrophic Lateral Sclerosis 18,Amyotrophic Lateral Sclerosis 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Giant Axonal Neuropathy 2,Amyotrophic Lateral Sclerosis 8,Lateral Sclerosis,Motor Neuron Disease,Hereditary Spastic Paraplegia,Multisystem Proteinopathy,Spinocerebellar Ataxia 1,Dementia,Amyotrophic Lateral Sclerosis 4, Juvenile,Progressive Muscular Atrophy,Pick Disease Of Brain,Autosomal Dominant Cerebellar Ataxia,Amyotrophic Lateral Sclerosis 19,Disease Of Mental Health,Dermatopathia Pigmentosa Reticularis,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4,Spinocerebellar Ataxia 2,Amyotrophic Lateral Sclerosis 15 With Or Without Frontotemporal Dementia,Amyotrophic Lateral Sclerosis 9,Brown-Vialetto-Van Laere Syndrome,Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia,Amyotrophic Lateral Sclerosis 16, Juvenile,Fragile X-Associated Tremor/Ataxia Syndrome,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia,Amyotrophic Lateral Sclerosis Type 6,Amyotrophic Lateral Sclerosis Type 12,Amyotrophic Lateral Sclerosis Type 14,Amyotrophic Lateral Sclerosis Type 15,Frontotemporal Dementia

Stomatitis,Myoclonic Epilepsy Of Lafora

Parkinson Disease, Late-Onset

Myopathy,Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency,Autoinflammation, Panniculitis, And Dermatosis Syndrome,Hepatitis B,Frontometaphyseal Dysplasia,Glycogen Storage Disease,Glycogen Storage Disease Iv,Polyglucosan Body Myopathy 1 With Or Without Immunodeficiency,Tooth Agenesis,Incontinentia Pigmenti,Myoclonic Epilepsy Of Lafora

Alzheimer Disease,Submucosal Cleft Palate,Cleft Hard Palate,Parkinson Disease, Late-Onset,Patella, Chondromalacia Of,Pick Disease Of Brain,Xeroderma Pigmentosum, Complementation Group C,Cleft Soft Palate,Encephalopathy, Familial, With Neuroserpin Inclusion Bodies,Smith-Magenis Syndrome,Down Syndrome,Uvula, Bifid,Leukodystrophy, Hypomyelinating, 7, With Or Without Oligodontia And/Or Hypogonadotropic Hypogonadism,Mulibrey Nanism,Myoclonic Epilepsy Of Lafora

Brachydactyly, Type A1