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Nume Neuronitis
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Clasificare anatomică Malacards Boli neuronale

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Boli A-Z 46,xy Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy Aarskog-Scott Syndrome Ablepharon-Macrostomia Syndrome Acardia Aceruloplasminemia Achalasia Achalasia, Familial Esophageal Achromatopsia Acoustic Neuroma Acrodermatitis Enteropathica, Zinc-Deficiency Type Acromegaly Acute Cervicitis Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion Acute Leukemia of Ambiguous Lineage Acute Mountain Sickness Acute Myocarditis Acute Pancreatitis Acute Pandysautonomia Acute Transverse Myelitis Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of Adams-Oliver Syndrome Adenocarcinoma Adenohypophysitis Adenoiditis Adenoma Adie Pupil Adjustment Disorder Adrenoleukodystrophy Adrenomyeloneuropathy Adult Mesoblastic Nephroma Adult Neuronal Ceroid Lipofuscinosis Adult Polyglucosan Body Disease Adult T-Cell Leukemia Agammaglobulinemia Age-Related Hearing Loss Aging Aids Dementia Complex Al Amyloidosis Aland Island Eye Disease Albinism Albinism, Ocular, Type I Alcohol Abuse Alcohol Dependence Alexander Disease Alexithymia Allan-Herndon-Dudley Syndrome Allergic Encephalomyelitis Allergic Hypersensitivity Disease Allergic Rhinitis Alobar Holoprosencephaly Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alopecia Universalis Congenita Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amblyopia Amyloid Neuropathy Amyloidosis Amyloidosis, Primary Localized Cutaneous, 1 Amyotrophic Lateral Sclerosis 1 Amyotrophic Lateral Sclerosis 2, Juvenile Amyotrophy, Monomelic Anaplastic Ganglioglioma Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome Anencephaly Aneurysm Angelman Syndrome Angel-Shaped Phalangoepiphyseal Dysplasia Angina Pectoris Angioedema Induced by Ace Inhibitors Anhidrosis Aniridia 1 Anisometropia Anorexia Nervosa 1 Anosmia Anovulation Anoxia Antigen Defined by Monoclonal Antibody Aj9 Antiphospholipid Syndrome Aphasia Apocrine Gland Secretion, Variation in Appendicitis Apraxia Arachnoid Cysts Arachnoiditis Arteries, Anomalies of Arteriovenous Malformation Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 5 Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Aspartylglucosaminuria Asthma Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Ataxia-Telangiectasia Atrial Fibrillation Attention Deficit-Hyperactivity Disorder Audiogenic Seizures Aural Atresia, Congenital Autism Autism Spectrum Disorder Autoimmune Autonomic Ganglionopathy Autoimmune Disease of Gastrointestinal Tract Autoimmune Encephalitis Autoimmune Inner Ear Disease Autoimmune Polyendocrine Syndrome Autoimmune Polyendocrine Syndrome Type 1 Autoimmune Polyglandular Syndrome Type 3 Autonomic Neuropathy Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Axonal Neuropathy Ayme-Gripp Syndrome Back Pain Bacterial Meningitis Band Heterotopia Bardet-Biedl Syndrome Bardet-Biedl Syndrome 8 Basal Cell Carcinoma B-Cell Lymphomas Behavioral Variant of Frontotemporal Dementia Benign Paroxysmal Positional Nystagmus Bipolar Disorder Bipolar I Disorder Bladder Cancer Bleeding Disorder, Platelet-Type, 11 Blepharospasm Blood Group--Ahonen Blood Group, Dombrock System Blood Group, Gerbich System Blood Group, I System Blood Group--Rhesus System E Polypeptide Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Bone Cancer Bone Fracture Bone Inflammation Disease Borderline Personality Disorder Borna Disease Bornholm Eye Disease Brachymorphism-Onychodysplasia-Dysphalangism Syndrome Brain Compression Brain Edema Brain Germinoma Brain Injury Brain Ischemia Breast Adenocarcinoma Breast Cancer Brooke-Spiegler Syndrome Brown-Vialetto-Van Laere Syndrome Brugada Syndrome Bullous Pemphigoid Burns Buruli Ulcer Camptocormism Canavan Disease Cardiac Arrest Carotid Artery Disease Carotid Artery Occlusion Carotid Artery Thrombosis Carotid Stenosis Cataract Cataract 40 Cataract 5, Multiple Types Cataract, Total Congenital Causalgia Cavernous Malformation Cd45 Deficiency Cdkl5-Related Disorder Central Nervous System Disease Central Nervous System Germinoma Central Nervous System Origin Vertigo Central Nervous System Vasculitis Central Neurocytoma Cerebellar Ataxia, Cayman Type Cerebellar Atrophy, Developmental Delay, and Seizures Cerebellar Degeneration Cerebellar Disease Cerebellar Hypoplasia Cerebellar Medulloblastoma Cerebral Arterial Disease Cerebral Artery Occlusion Cerebral Atrophy Cerebral Cavernous Malformations Cerebral Degeneration Cerebral Hemorrhage Cerebral Hypoxia Cerebral Palsy Cerebritis Cerebrovascular Disease Ceroid Lipofuscinosis, Neuronal, 1 Ceroid Lipofuscinosis, Neuronal, 10 Ceroid Lipofuscinosis, Neuronal, 2 Ceroid Lipofuscinosis, Neuronal, 3 Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive Ceroid Lipofuscinosis, Neuronal, 5 Ceroid Lipofuscinosis, Neuronal, 6 Ceroid Lipofuscinosis, Neuronal, 7 Ceroid Lipofuscinosis, Neuronal, 8, Northern Epilepsy Variant Cervical Dystonia Cervicitis Chagas Disease Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease, Type 4a Chemical Colitis Chikungunya Childhood Absence Epilepsy Childhood Apraxia of Speech Childhood Myocerebrohepatopathy Spectrum Childhood-Onset Schizophrenia Chlamydia Choanal Atresia, Posterior Cholera Cholestasis Chondrodysplasia Punctata Syndrome Chops Syndrome Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choroideremia Choroiditis Christianson Syndrome Chromosomal Triplication Chromosome 15q Duplication Chromosome 16 Trisomy Chronic Enteropathy Associated with Slco2a1 Gene Chronic Fatigue Syndrome Chronic Inflammatory Demyelinating Polyneuropathy Chronic Mountain Sickness Chronic Pain Chronic Progressive External Ophthalmoplegia Ciliopathy Clear Cell Renal Cell Carcinoma Clear Cell Sarcoma Cleft Larynx, Posterior Cleft Lip Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly Cluster Headache Cocaine Abuse Cocaine Antenatal Exposure Cockayne Syndrome Cockayne Syndrome B Coffin-Lowry Syndrome Cognitive Function 1, Social Colitis Colonic Atresia Colonic Pseudo-Obstruction Colorblindness, Partial, Protan Series Colorectal Cancer Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complex Regional Pain Syndrome Congenital Cytomegalovirus Congenital Hypothyroidism Congenital Lymphedema Congenital Non-Communicating Hydrocephalus Congenital Nystagmus Congestive Heart Failure Conjunctivitis Constipation Contact Dermatitis Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia Cortical Blindness Cortical Dysplasia, Complex, with Other Brain Malformations 7 Corticobasal Degeneration Costello Syndrome Cranial Nerve Palsy Crest Syndrome Creutzfeldt-Jakob Disease Cryoglobulinemia Currarino Syndrome Cystic Fibrosis Cystitis Cytomegalovirus Infection Cytomegalovirus Retinitis Cytoplasmic Body Myopathy Danon Disease Dementia Demyelinating Disease Demyelinating Polyneuropathy Dentatorubral-Pallidoluysian Atrophy Dermatitis Developmental Coordination Disorder Diabetes Insipidus Diabetes Mellitus Diabetic Encephalopathy Diabetic Neuropathy Diabetic Polyneuropathy Diarrhea Differentiating Neuroblastoma Diffuse Large B-Cell Lymphoma Diphtheria Dirofilariasis Distal Arthrogryposis Distal Hereditary Motor Neuropathies Donnai-Barrow Syndrome Dopamine Beta-Hydroxylase Deficiency, Congenital Down Syndrome Doxorubicin Induced Cardiomyopathy Drug Dependence Drug Induced Dyskinesia Duodenitis Dwarfism Dysautonomia Dysembryoplastic Neuroepithelial Tumor Dysentery Dyslexia Dyspepsia Dysphagia Dystonia Dystonia 4, Torsion, Autosomal Dominant Early-Onset Generalized Limb-Onset Dystonia Early-Onset Schizophrenia Ectropion Embryonal Carcinoma Encephalitis Encephalocele Encephalomalacia Encephalopathy Endogenous Depression Endometriosis Endotheliitis Eosinophilia-Myalgia Syndrome Eosinophilic Fasciitis Eosinophilic Pustular Folliculitis Ependymoma Epidermolysis Bullosa Pruriginosa Epilepsy Epilepsy, Nocturnal Frontal Lobe, 4 Epileptic Encephalopathy, Early Infantile, 6 Episodic Ataxia Episodic Ataxia, Type 1 Episodic Ataxia, Type 2 Epithelial Recurrent Erosion Dystrophy Epithelioid Leiomyosarcoma Erythromelalgia Esophageal Atresia Essential Tremor Ewing Sarcoma Exencephaly Extrahepatic Cholestasis Fabry Disease Facial Paralysis Familial Hemiplegic Migraine Fanconi Anemia, Complementation Group E Fatal Familial Insomnia Fazio-Londe Disease Febrile Seizures Fecal Incontinence Femoral-Facial Syndrome Fetal Akinesia Deformation Sequence Fetal Alcohol Spectrum Disorder Fetal Alcohol Syndrome Fibromatosis, Gingival, 2 Fibrosarcoma Fibrous Histiocytoma Focal Epilepsy Folliculitis Fragile X-Associated Tremor/ataxia Syndrome Fragile X Syndrome Friedreich Ataxia 1 Frontotemporal Dementia Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 Frontotemporal Dementia, Chromosome 3-Linked Frozen Shoulder Fructose Utilization Fundus Albipunctatus Galactose Epimerase Deficiency Galactosialidosis Gangliocytoma Ganglioglioma Ganglioneuroblastoma Gardner-Diamond Syndrome Gastric Ulcer Gastrointestinal Neuroendocrine Tumor Gastrointestinal Stromal Tumor Gastroparesis Gastroschisis Gaucher Disease, Type Iii Generalized Epilepsy with Febrile Seizures Plus Generalized Epilepsy with Febrile Seizures Plus, Type 2 Geniculate Ganglionitis Geniculate Herpes Zoster Germ Cells Tumors Gerstmann Syndrome Giant Axonal Neuropathy Giant Cell Glioblastoma Gigantism Gilles De La Tourette Syndrome Gitelman Syndrome Glaucoma-Related Pigment Dispersion Syndrome Glioblastoma Glioblastoma Multiforme Glioma Gliomatosis Cerebri Gliosarcoma Glucose Intolerance Glucose Transporter Type 1 Deficiency Syndrome Goldberg-Shprintzen Syndrome Gout Granulomatous Myositis Griscelli Syndrome Guillain-Barre Syndrome Guillain-Barre Syndrome, Familial Haemophilus Influenzae Haim-Munk Syndrome Hair Disease Hairy Nose Tip Harlequin Syndrome Headache Head Injury Helix Syndrome Hematopoietic Stem Cell Transplantation Hemidystonia Hemifacial Spasm Hemihyperplasia, Isolated Hemimegalencephaly Hemiplegia Hemiplegic Migraine Hemochromatosis, Neonatal Hemophagocytic Lymphohistiocytosis Hemorrhagic Fever Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatitis Hepatocellular Carcinoma Hereditary Sensory Neuropathy Hereditary Spastic Paraplegia Hereditary Wilms' Tumor Hermansky-Pudlak Syndrome Heroin Dependence Herpes Gestationis Herpes Simplex Herpes Simplex Encephalitis Herpes Zoster Herpes Zoster Ophthalmicus Histiocytoma Holoprosencephaly Holoprosencephaly 3 Horns in Sheep Human Coronavirus Sensitivity Human Immunodeficiency Virus Type 1 Human T-Cell Leukemia Virus Type 1 Huntington Disease Hydrocephalus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperaldosteronism, Familial, Type I Hyperandrogenism Hypercholesterolemia, Autosomal Dominant, 3 Hyperekplexia Hyperglycemia Hypermethioninemia Hyperparathyroidism Hyperphenylalaninemia Hyperphosphatemia Hyperprolactinemia Hypersomnia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypertonia Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertrophic Pyloric Stenosis Hypochondroplasia Hypoganglionosis Hypoglycemia Hypoglycemic Coma Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypomelanosis of Ito Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatasia, Adult Hypophosphatasia, Infantile Hypoplastic Left Heart Syndrome 1 Hypothalamic Hamartomas Hypotonia Hypotonia-Cystinuria Syndrome Hypoxia Ichthyosis Ichthyosis, Congenital, Autosomal Recessive 11 Ichthyosis Prematurity Syndrome Ideomotor Apraxia Idiopathic Achalasia Idiopathic Scoliosis Ileitis Immunoglobulin E Concentration, Serum Inclusion Body Myositis Incontinentia Pigmenti Infantile Epileptic Encephalopathy Infertility Inflammatory Bowel Disease Influenza Insulin-Like Growth Factor I Intellectual Disability-Developmental Delay-Contractures Syndrome Intermittent Claudication Internuclear Ophthalmoplegia Intestinal Atresia Intestinal Disease Intestinal Pseudo-Obstruction Intestinal Schistosomiasis Intracranial Aneurysm Intracranial Embolism Intracranial Hypertension Iris Pattern Irritable Bowel Syndrome Ischemia Ischemic Optic Neuropathy Ischemic Retinopathy Isolated Growth Hormone Deficiency, Type Ia Isolated Optic Neuritis Japanese Encephalitis Juvenile Amyotrophic Lateral Sclerosis Juvenile Huntington Disease Kallmann Syndrome Kernicterus Kleefstra Syndrome Knobloch Syndrome Krabbe Disease Lactic Acidosis Lambert-Eaton Myasthenic Syndrome Laryngitis Lateral Medullary Syndrome Lateral Sclerosis Lathyrism Learning Disability Left Ventricular Noncompaction Legius Syndrome Leigh Syndrome Leiomyosarcoma Lennox-Gastaut Syndrome Lesch-Nyhan Syndrome Leukemia Leukodystrophy Leukodystrophy, Hypomyelinating, 5 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leukomalacia Leukostasis Lewis-Sumner Syndrome Limb-Girdle Muscular Dystrophy Limbic Encephalitis Lipid Storage Disease Lissencephaly Lissencephaly 1 Lissencephaly 4 Lissencephaly, X-Linked, 1 Listeriosis Liver Cirrhosis Liver Disease Locked-in Syndrome Louping Ill Lung Cancer Lung Disease Lupus Erythematosus Lyme Disease Lymphangiectasis Lymphedema Lymphocytic Choriomeningitis Lymphoma Lymphopenia Lysosomal Storage Disease Machado-Joseph Disease Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Madras Motor Neuron Disease Major Affective Disorder 2 Major Affective Disorder 8 Major Affective Disorder 9 Malaria Malignant Germ Cell Tumor Malignant Glioma Malignant Hypertension Malignant Hyperthermia Malignant Hyperthermia Susceptibility Malignant Spiradenoma Mannosidosis Mannosidosis, Alpha B, Lysosomal Maple Syrup Urine Disease Marchiafava Bignami Disease Mast Syndrome Mature Teratoma Mbd5 Haploinsufficiency Measles Mediastinitis Medullary Sponge Kidney Medulloblastoma Medullomyoblastoma Megacolon Megaesophagus Megalencephaly Melancholia Melanoma Melkersson-Rosenthal Syndrome Melorheostosis, Isolated Meningitis Meningoencephalitis Menkes Disease Mercury Poisoning Merkel Cell Carcinoma Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis Metabolic Acidosis Metachromatic Leukodystrophy Microcephalic Osteodysplastic Primordial Dwarfism, Type I Microcephaly Microcephaly, Epilepsy, and Diabetes Syndrome Microlissencephaly Microphthalmia Microtia-Anotia Migraine with or Without Aura 1 Migraine Without Aura Miller Fisher Syndrome Mini Stroke Mitochondrial Disorders Mitochondrial Dna Depletion Syndrome 4a Moebius Syndrome Monoclonal Paraproteinemia Mononeuropathy Monosomy 21 Mood Disorder Morning Glory Syndrome Morphine Dependence Motion Sickness Motor Neuron Disease Mucolipidosis Iv Mucopolysaccharidoses Mucopolysaccharidosis Iii Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Iiib Mucopolysaccharidosis, Type Vii Mucositis Muenke Syndrome Multifocal Motor Neuropathy Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Multiple Sclerosis 5 Multiple System Atrophy 1 Multisystemic Smooth Muscle Dysfunction Syndrome Mumps Mungan Syndrome Muscular Atrophy Muscular Dystrophy Musical Perfect Pitch Mutism Myasthenia Gravis Myelitis Myeloma, Multiple Myelomeningocele Myocardial Infarction Myocarditis Myoclonic Epilepsy of Infancy Myoclonus Myoclonus Epilepsy Myopathy Myopathy, Myofibrillar, 3 Myopia Myositis Myotonia Myotonic Dystrophy N Acetyltransferase Deficiency Nance-Horan Syndrome Narcolepsy Necrotizing Autoimmune Myopathy Neonatal Hypothyroidism Neonatal Hypoxic and Ischemic Brain Injury Neonatal Meningitis Neonatal Stroke Nervous System Cancer Nervous System Disease Neu-Laxova Syndrome 1 Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neuraminidase Deficiency Neuritis Neuroaxonal Dystrophy Neuroblastoma Neurodegeneration with Brain Iron Accumulation Neurodegeneration with Brain Iron Accumulation 2a Neuroendocrine Tumor Neurofibromatosis, Type I Neurofibromatosis, Type Iv, of Riccardi Neurogenic Bladder Neurogenic Bowel Neurogenic Hypertension Neuroleptic Malignant Syndrome Neuroma Neuromuscular Disease Neuromuscular Junction Disease Neuromyelitis Optica Neuronal Ceroid-Lipofuscinoses Neuronal Ceroid Lipofuscinosis Neuronal Intestinal Dysplasia Neuronal Intestinal Dysplasia, Type B Neuronal Intranuclear Inclusion Disease Neuronal Migration Disorders Neuronopathy, Distal Hereditary Motor, Type Viib Neuropathy Neuropathy, Hereditary Sensory and Autonomic, Type Iii Neuroretinitis Neutrophil Actin Dysfunction Neutrophilic Dermatosis, Acute Febrile Nevus Comedonicus Nicolaides-Baraitser Syndrome Niemann-Pick Disease Niemann-Pick Disease, Type C1 Nijmegen Breakage Syndrome Nodular Neuronal Heterotopia Non-Involuting Congenital Hemangioma Obsessive-Compulsive Disorder Obstructive Hydrocephalus Obstructive Jaundice Occipital Horn Syndrome Ocular Albinism Ocular Dominance Ocular Motor Apraxia Oculocutaneous Albinism Oculopharyngeal Muscular Dystrophy Oligodendroglioma Oliver Syndrome Olivopontocerebellar Atrophy Omsk Hemorrhagic Fever Opiate Dependence Opioid Addiction Opsoclonus-Myoclonus Syndrome Optic Atrophy 1 Optic Neuritis Oral Cancer Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteoglophonic Dysplasia Osteopetrosis Ovarian Cancer Overhydrated Hereditary Stomatocytosis Pachygyria Pachyonychia Congenita 1 Pachyonychia Congenita 2 Pachyonychia Congenita 3 Paine Syndrome Pancreatic Cancer Pancreatitis Pandas Panic Disorder Papillary Glioneuronal Tumors Papillon-Lefevre Syndrome Paraneoplastic Cerebellar Degeneration Paraneoplastic Neurologic Disorders Paraneoplastic Syndromes Paraplegia Parathyroid Adenoma Paresthesia Parkinson Disease 13, Autosomal Dominant Parkinson Disease 15, Autosomal Recessive Early-Onset Parkinson Disease 2, Autosomal Recessive Juvenile Parkinson Disease 7, Autosomal Recessive Early-Onset Paroxysmal Extreme Pain Disorder Patent Foramen Ovale Pathological Gambling Pediatric Ovarian Dysgerminoma Peho Syndrome Pelizaeus-Merzbacher Disease Pepck 1 Deficiency Pericarditis Pericoronitis Periodontitis Periodontitis, Aggressive, 1 Perioral Myoclonia with Absences Peritonitis Periventricular Leukomalacia Periventricular Nodular Heterotopia Peroneal Neuropathy Peroxisomal Biogenesis Disorders Perry Syndrome Persistent Idiopathic Facial Pain Persistent Vegetative State Personality Disorder Pertussis Pfeiffer Syndrome Phaeochromocytoma Pharyngitis Phelan-Mcdermid Syndrome Phenylketonuria Pheochromocytoma Pick Disease of Brain Pineoblastoma Pineocytoma Pitt-Hopkins Syndrome Pituitary Adenoma Pituitary Hormone Deficiency, Combined, 2 Pituitary Hypoplasia Pituitary Tumors Placental Insufficiency Plasmacytoma Pleomorphic Xanthoastrocytoma Pleurisy Pneumococcal Meningitis Pneumonia Pneumothorax, Primary Spontaneous Poikiloderma with Neutropenia Poliomyelitis Polycystic Kidney Disease Polykaryocytosis Inducer Polymicrogyria Polymicrogyria, Bilateral Perisylvian, X-Linked Polymorphic Reticulosis Polymyositis Polyneuropathy Polyradiculoneuropathy Pontine Tegmental Cap Dysplasia Pontocerebellar Hypoplasia Postherpetic Neuralgia Postpartum Psychosis Posttransplant Acute Limbic Encephalitis Post-Traumatic Stress Disorder Prader-Willi Syndrome Precocious Puberty Premature Centromere Division Premature Chromatid Separation Trait Premature Ejaculation Prieto X-Linked Mental Retardation Syndrome Primary Cerebellar Degeneration Primary Hyperparathyroidism Prion Disease Progressive Bulbar Palsy Progressive Encephalomyelitis with Rigidity and Myoclonus Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Progressive Multifocal Leukoencephalopathy Progressive Muscular Atrophy Progressive Myoclonus Epilepsy Prolidase Deficiency Propionic Acidemia Prostate Cancer Prostatitis Protocadherin-Alpha Gene Cluster Pseudobulbar Affect Pseudobulbar Palsy Psoriasis Psoriasis 13 Pulmonary Disease, Chronic Obstructive Pulpitis Pure Autonomic Failure Pyloric Stenosis Pyridoxine Deficiency Rabies Radiculopathy Raine Syndrome Rasmussen Encephalitis Rasmussen Subacute Encephalitis Reactive Angioendotheliomatosis Refsum Disease, Classic Relapsing-Remitting Multiple Sclerosis Rem Sleep Behavior Disorder Renal Glucosuria Renal Hypertension Renal Hypoplasia Renal Nutcracker Syndrome Renovascular Hypertension Renpenning Syndrome 1 Restless Legs Syndrome Retinal Degeneration Retinal Detachment Retinal Disease Retinal Ischemia Retinitis Retinitis Pigmentosa Retinoblastoma Rett Syndrome Reunion Island Larsen Syndrome Rhabdomyosarcoma Rheumatoid Arthritis Rhinitis Rhizomelic Chondrodysplasia Punctata Riboflavin Transporter Deficiency Neuronopathy Ring Chromosome 1 Ring Chromosome 2 Ring Chromosome 7 Roberts Syndrome Root Resorption Rosacea Rosai-Dorfman Disease Salivary Gland Adenoma, Pleomorphic Salt and Pepper Developmental Regression Syndrome Sandhoff Disease Sarcoma Schistosomiasis Schizoaffective Disorder Schizophrenia Schizophrenia 1 Schopf-Schulz-Passarge Syndrome Sciatic Neuropathy Sclerosing Cholangitis, Neonatal Scn8a Encephalopathy Scoliosis Scoliosis, Isolated 1 Scotoma Sc Phocomelia Syndrome Scrapie Sebastian Syndrome Secondary Progressive Multiple Sclerosis Seizure Disorder Seizures, Benign Familial Neonatal, 1 Semantic Dementia Semilobar Holoprosencephaly Seminoma Sensorineural Hearing Loss Severe Acute Respiratory Syndrome Severe Combined Immunodeficiency Shaken Baby Syndrome Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Siderosis Sinusitis Skin Tag Sleep Apnea Sleep Disorder Sleeping Sickness Small Cell Cancer of the Lung Small Cell Carcinoma Small Cell Neuroendocrine Carcinoma Smith-Kingsmore Syndrome Smith-Lemli-Opitz Syndrome Smoking As a Quantitative Trait Locus 3 Space Motion Sickness Spastic Diplegia Spastic Hemiplegia Spasticity Spastic Paraparesis Spastic Paraplegia 11 Spastic Paraplegia 20, Autosomal Recessive Spastic Paraplegia, Ataxia, and Mental Retardation Spina Bifida Aperta Spina Bifida Occulta Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinal Cord Injury Spinal Muscular Atrophy Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Spinal Muscular Atrophy, Type Ii Spinal Muscular Atrophy, Type Iii Spinal Shock Spindle Cell Hemangioma Spindle Cell Sarcoma Spinocerebellar Ataxia 12 Spinocerebellar Ataxia 17 Spinocerebellar Ataxia 36 Spinocerebellar Ataxia 7 Spinocerebellar Ataxia, Autosomal Recessive 7 Spinocerebellar Degeneration Spiradenoma Spitz Nevus Spondyloocular Syndrome Spondylosis Squamous Cell Carcinoma Stachybotrys Chartarum Status Epilepticus Stiff-Person Syndrome St. Louis Encephalitis Stomatitis Strabismus Streptococcal Meningitis Striatal Degeneration, Autosomal Dominant 2 Striatonigral Degeneration Sturge-Weber Syndrome Stuttering Subcortical Band Heterotopia Sudden Infant Death Syndrome Sulfite Oxidase Deficiency, Isolated Superficial Siderosis Suppressor of Tumorigenicity 3 Sveinsson Chorioretinal Atrophy Swayback Sydenham Chorea Synesthesia Synucleinopathy Syringomyelia Systemic Lupus Erythematosus Takenouchi-Kosaki Syndrome Tangier Disease Tardive Dyskinesia Tarp Syndrome Tay-Sachs Disease T-Cell Leukemia Temporal Arteritis Temporal Lobe Epilepsy Tendinopathy Tendinosis Teratocarcinoma Teratoma Testicular Cancer Testicular Germ Cell Tumor Testicular Germ Cell Tumor 1 Testicular Regression Syndrome Tetanus Tetanus Neonatorum Tethered Cord Syndrome Tetrahydrobiopterin Deficiency Tetraploidy Three M Syndrome 1 Thrombosis Thymic Hyperplasia Thymoma Thyroiditis Thyrotropin-Releasing Hormone Deficiency Tic Disorder Tick-Borne Encephalitis Timothy Syndrome Tooth Disease Toxic Encephalopathy Toxic Megacolon Toxic Oil Syndrome Toxoplasmoză Tracheoesophageal Fistula Transient Arthritis Transient Cerebral Ischemia Transient Global Amnesia Transitional Cell Carcinoma Transverse Myelitis Traumatic Brain Injury Tremor Trichohepatoenteric Syndrome 1 Trypanosomiasis Trypanosomiasis, Human East-African Tuberculous Meningitis Tuberous Sclerosis Tubulin, Beta Tumor Suppressor Gene on Chromosome 11 Turner Syndrome Ulcerative Colitis Ulnar Neuropathy Uremia Uremic Pruritus Urethral Stricture Urethritis Usher Syndrome Uterine Sarcoma Van Der Woude Syndrome 1 Van Maldergem Syndrome Vascular Dementia Vascular Disease Vasomotor Rhinitis Venezuelan Equine Encephalitis Vertebral Artery Occlusion Vestibular Neuronitis Vestibular Nystagmus Viral Encephalitis Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Walker-Warburg Syndrome Wallerian Degeneration Warburg Micro Syndrome Warburg Micro Syndrome 1 Weber Syndrome Werner Syndrome Wernicke Encephalopathy Wernicke-Korsakoff Syndrome Western Equine Encephalitis West Nile Encephalitis West Nile Virus West Syndrome Williams-Beuren Syndrome Wilms Tumor 6 Wiskott-Aldrich Syndrome Wolfram Syndrome Wolfram Syndrome 1 Yellow Fever Zellweger Syndrome