Eyelid Carcinoma,Orofacial Cleft 4,Split Hand-Foot Malformation,Isolated Split Hand-Split Foot Malformation,Split-Hand/Foot Malformation 1 With Sensorineural Hearing Loss, Autosomal Recessive,Skin Squamous Cell Carcinoma,Split-Hand/Foot Malformation 6,Paranoid Personality Disorder,Shoulder Impingement Syndrome,Fanconi Anemia, Complementation Group A,Split-Hand/Foot Malformation 4,Split-Hand/Foot Malformation 1,Citrullinemia, Type Ii, Neonatal-Onset,Chromosome 2q35 Duplication Syndrome,Split-Hand/Foot Malformation 5,Split-Hand/Foot Malformation 3,Attention Deficit-Hyperactivity Disorder,Split-Hand/Foot Malformation 2

Alzheimer Disease,Angelman Syndrome,Cystic Fibrosis,Cholera,Encephalopathy, Familial, With Neuroserpin Inclusion Bodies,Inflammatory Bowel Disease

Cystic Fibrosis

Alzheimer Disease,Cystic Fibrosis,Ehrlichiosis,Pheochromocytoma

Muscular Disease,Amyotrophic Lateral Sclerosis 6 With Or Without Frontotemporal Dementia,Zellweger Syndrome,Supranuclear Palsy, Progressive, 1,Retinitis Pigmentosa,Myopathy,Myofibrillar Myopathy,Muscle Tissue Disease,Neuromuscular Disease,Alzheimer Disease,Nominal Aphasia,Amyotrophic Lateral Sclerosis 1,Myositis,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Early-Onset, Autosomal Dominant Alzheimer Disease,Amyotrophic Lateral Sclerosis 8,Lateral Sclerosis,Motor Neuron Disease,Autosomal Dominant Limb-Girdle Muscular Dystrophy,Muscular Dystrophy,Movement Disease,Progressive Non-Fluent Aphasia,Dyscalculia,Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone With Or Without Frontotemporal Dementia 1,Hereditary Spastic Paraplegia,Cystic Fibrosis,Machado-Joseph Disease,Spastic Paraplegia-Paget Disease Of Bone Syndrome,Adult-Onset Distal Myopathy Due To Vcp Mutation,Multisystem Proteinopathy,Dementia,Paget'S Disease Of Bone,Cockayne Syndrome,Alexia,Inclusion Body Myopathy With Early-Onset Paget Disease With Or Without Frontotemporal Dementia 1,Charcot-Marie-Tooth Disease,Parkinson Disease, Late-Onset,Perry Syndrome,Speech And Communication Disorders,Progressive Muscular Atrophy,Tooth Disease,Pick Disease Of Brain,Werner Syndrome,Autosomal Dominant Cerebellar Ataxia,Neuronal Ceroid Lipofuscinosis,Mammary Paget'S Disease,Breast Adenocarcinoma,Disease Of Mental Health,Dementia, Lewy Body,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 6,Fanconi Anemia, Complementation Group G,Nonaka Myopathy,Alzheimer Disease 7,Amyotrophic Lateral Sclerosis 16, Juvenile,Ehlers-Danlos Syndrome, Spondylodysplastic Type, 3,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia,Aphasia,Writing Disorder,Inclusion Body Myositis,Associative Agnosia,Amyotrophic Lateral Sclerosis Type 6,Amyotrophic Lateral Sclerosis Type 14,Agraphia,Charcot-Marie-Tooth Disease, Axonal, Type 2e,Frontotemporal Dementia,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7

Angelman Syndrome,Cystic Fibrosis,Autosomal Dominant Cerebellar Ataxia

Angelman Syndrome,Cystic Fibrosis

Progressive Myoclonus Epilepsy,Dystonia 9,Spasticity,Epilepsy,Optic Nerve Disease,Episodic Ataxia,Chronic Progressive External Ophthalmoplegia,Hereditary Spastic Paraplegia,Cerebellar Ataxia Type 41,Cerebellar Ataxia Type 48,Choreatic Disease,Sensorineural Hearing Loss,Spastic Paraparesis,Cerebellar Disease,Dystonia,Neuropathy,Early Myoclonic Encephalopathy,Spinocerebellar Ataxia 30,Spinocerebellar Ataxia, Autosomal Recessive 14,Myoclonus,Spinocerebellar Ataxia 29,Alacrima, Achalasia, And Mental Retardation Syndrome,Autosomal Dominant Cerebellar Ataxia,Disease Of Mental Health,Spinocerebellar Ataxia 28,Optic Atrophy With Or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, And Neuropathy,Dentatorubral-Pallidoluysian Atrophy,Aceruloplasminemia,Optic Atrophy 5,Spinocerebellar Ataxia, Autosomal Recessive 8,Optic Atrophy 9,Spinocerebellar Ataxia 15,Perrault Syndrome,Spastic Ataxia 5, Autosomal Recessive,Spastic Ataxia 4,Spastic Ataxia 5,Hereditary Ataxia,Spastic Ataxia,Spastic Paraplegia 7, Autosomal Recessive,Spinocerebellar Ataxia 21,Spinocerebellar Ataxia 18,Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis,Optic Atrophy 10 With Or Without Ataxia, Mental Retardation, And Seizures,Ptosis,Optic Atrophy 12,Striatal Degeneration, Autosomal Dominant 2,Kearns-Sayre Syndrome,3-Methylglutaconic Aciduria, Type Iii

Histrionic Personality Disorder