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Nume Neuropathy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Polyneuropathy, unspecified
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli neuronale
Boli din aceeaşi familie Autoimmune Neuropathy; Hereditary Neuropathies; Hereditary Type 1 Neuropathy; Hereditary Type 2 Neuropathy

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Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 46,xy Partial Gonadal Dysgenesis 48,xxyy Syndrome Aarskog-Scott Syndrome Abducens Palsy Abetalipoproteinemia Aceruloplasminemia Achalasia Achalasia-Addisonianism-Alacrima Syndrome Acoustic Neuroma Acquired Immunodeficiency Syndrome Acrocallosal Syndrome Acrodermatitis Acrodermatitis Chronica Atrophicans Acromegaly Acute Closed-Angle Glaucoma Acute Disseminated Encephalomyelitis Acute Lymphocytic Leukemia Acute Monoblastic Leukemia Acute Motor and Sensory Axonal Neuropathy Acute Motor Axonal Neuropathy Acute Myocardial Infarction Acute Pancreatitis Acute Porphyria Acute Promyelocytic Leukemia Acute Respiratory Distress Syndrome Acute Sensory Ataxic Neuropathy Acute Transverse Myelitis Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of Adenocarcinoma Adenoma Adie Pupil Adrenoleukodystrophy Adrenomyeloneuropathy Adult T-Cell Leukemia African Tick-Bite Fever Agenesis of the Corpus Callosum with Peripheral Neuropathy Aging Agnosia Alagille Syndrome 1 Al Amyloidosis Aland Island Eye Disease Alcohol Abuse Alcohol Dependence Alcoholic Liver Cirrhosis Alcoholic Neuropathy Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 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 Amaurosis Fugax Amblyopia Amyloid Neuropathy Amyloidosis Amyloidosis, Finnish Type Amyloidosis, Hereditary, Transthyretin-Related Amyotrophic Neuralgia Amyotrophy, Hereditary Neuralgic Amyotrophy, Monomelic Anaplastic Large Cell Lymphoma Anauxetic Dysplasia 1 Anca-Associated Vasculitis Aneurysm Aneurysmal Bone Cysts Angel-Shaped Phalangoepiphyseal Dysplasia Angiofollicular Lymph Hyperplasia Angioid Streaks Angiomatosis Anhidrosis Aniridia 1 Anorexia Nervosa 1 Anosmia Anterior Compartment Syndrome Anterior Uveitis Antiphospholipid Syndrome Aortic Aneurysm Aortitis Aplasia Cutis Congenita Apraxia Arachnoid Cysts Arachnoiditis Arteries, Anomalies of Arteriovenous Fistula Arteriovenous Malformation Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 5 Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Arthropathy Asthma Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Ataxia with Vitamin E Deficiency Atrial Fibrillation Atrial Standstill Auditory Neuropathy, Autosomal Dominant, 1 Auditory Neuropathy Spectrum Disorder Australia Antigen Autism Autism Spectrum Disorder Autoimmune Autonomic Ganglionopathy Autoimmune Disease Autoimmune Neuropathy Autoimmune-Related Retinopathy and Optic Neuropathy Autoinflammation with Infantile Enterocolitis Autonomic Dysfunction Autonomic Neuropathy Autonomic Peripheral Neuropathy Autosomal Dominant Cerebellar Ataxia Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease Type B Autosomal Recessive Cerebellar Ataxia Avascular Necrosis of Femoral Head, Primary, 1 Axonal Neuropathy Baroreflex Failure Basal Cell Carcinoma B-Cell Expansion with Nfkb and T-Cell Anergy B-Cell Lymphomas Beriberi Biotinidase Deficiency Blau Syndrome Bleeding Disorder, Platelet-Type, 11 Blind Loop Syndrome Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blue Rubber Bleb Nevus 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 Fracture Bornholm Eye Disease Boylan Dew Greco Syndrome Brachial Plexus Neuritis Brachial Plexus Neuropathy Brain Edema Brain Injury Brainstem Auditory Evoked Responses Branchiootic Syndrome 1 Branch Retinal Artery Occlusion Breast Cancer Breast Reconstruction Bronchopneumonia Brooke-Spiegler Syndrome Brown-Vialetto-Van Laere Syndrome Brugada Syndrome Burkitt Lymphoma Burning Mouth Syndrome Burns Bursitis C1 Inhibitor Deficiency Calcific Tendinitis Calcinosis Calciphylaxis Camurati-Engelmann Disease Cancer-Associated Retinopathy Capillary Hemangioma Carcinoid Syndrome Carcinoid Tumors, Intestinal Cardiac Arrest Carnitine Deficiency, Systemic Primary Carotid Artery Dissection Carpal Tunnel Syndrome Castleman Disease Cataract Cataract 40 Cataract, Total Congenital Cat-Scratch Disease Cavernous Hemangioma Cavernous Sinus Thrombosis Celiac Disease 1 Cellulitis Central Nervous System Disease Central Nervous System Origin Vertigo Central Retinal Artery Occlusion Central Retinal Vein Occlusion Central Serous Chorioretinopathy Central Sleep Apnea Centronuclear Myopathy Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy and Sensorinural Hearing Loss Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome Cerebellar Degeneration Cerebellar Hypoplasia Cerebral Arteritis Cerebral Atrophy Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome Cerebral Lymphoma Cerebral Palsy Cerebral Palsy, Ataxic, Autosomal Recessive Cerebral Sarcoidosis Cerebritis Cerebrotendinous Xanthomatosis Cervicitis Chagas Disease Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease and Deafness Charcot-Marie-Tooth Disease, Axonal, Type 2b Charcot-Marie-Tooth Disease, Axonal, Type 2d Charcot-Marie-Tooth Disease, Axonal, Type 2e Charcot-Marie-Tooth Disease, Axonal, Type 2f Charcot-Marie-Tooth Disease, Axonal, Type 2t Charcot-Marie-Tooth Disease, Demyelinating, Type 1a Charcot-Marie-Tooth Disease, Demyelinating, Type 1b Charcot-Marie-Tooth Disease, Demyelinating, Type 1c Charcot-Marie-Tooth Disease, Demyelinating, Type 1d Charcot-Marie-Tooth Disease, Demyelinating, Type 1f Charcot-Marie-Tooth Disease, Demyelinating, Type 4f Charcot-Marie-Tooth Disease, Type 4a Charcot-Marie-Tooth Disease, Type 4b1 Charcot-Marie-Tooth Disease, Type 4c Charcot-Marie-Tooth Disease, Type 4d Charcot-Marie-Tooth Disease, Type 4h Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 Charcot-Marie-Tooth Disease, X-Linked Dominant, 6 Charcot-Marie-Tooth Disease, X-Linked Recessive, 3 Charcot-Marie-Tooth Hereditary Neuropathy Charcot-Marie-Tooth Neuropathy Type 1 Charcot-Marie-Tooth Neuropathy Type 2a Charcot-Marie-Tooth Neuropathy Type 2e/1f Charcot-Marie-Tooth Neuropathy Type 4j Charcot-Marie-Tooth Neuropathy X Type 1 Charcot-Marie-Tooth Neuropathy X Type 5 Chediak-Higashi Syndrome Cheilitis Cherubism Chiari Malformation Chikungunya Chlamydia Cholecystitis Cholera Chondroma Chordoid Meningioma Chordoma Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chorioretinitis Choroiditis Choroid Plexus Meningioma Chromosomal Triplication Chromosome 17p Duplication Chronic Graft Versus Host Disease Chronic Inflammatory Demyelinating Polyneuropathy Chronic Inflammatory Demyelinating Polyradiculoneuropathy Chronic Intestinal Pseudoobstruction Chronic Meningitis Chronic Myelomonocytic Leukemia Chronic Pain Chronic Progressive External Ophthalmoplegia Chronic Relapsing Inflammatory Optic Neuropathy Churg-Strauss Syndrome Chylomicron Retention Disease Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly Cocaine Abuse Cockayne Syndrome Cockayne Syndrome a Cold Agglutinin Disease Colitis Colon Adenocarcinoma Colonic Pseudo-Obstruction Colorectal Adenocarcinoma Colorectal Cancer Compartment Syndrome Complement Component 4, Partial Deficiency of Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complex Regional Pain Syndrome Conduct Disorder Cone Dystrophy Congenital Cataracts, Facial Dysmorphism, and Neuropathy Congenital Hypomyelination Neuropathy Connective Tissue Disease Constipation Corneal Dystrophy Corneal Edema Cortical Blindness Cramp-Fasciculation Syndrome Cranial Nerve Disease Cranial Nerve Palsy Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Crest Syndrome Creutzfeldt-Jakob Disease Cri-Du-Chat Syndrome Critical Illness Polyneuropathy Critical Limb Ischemia Crohn's Colitis Crohn's Disease Cryoglobulinemia Cutaneous Lupus Erythematosus Cyanide Poisoning Cyclic Vomiting Syndrome Cystic Fibrosis Cytomegalovirus Infection D-2-Hydroxyglutaric Aciduria 1 Dandy-Walker Syndrome D-Bifunctional Protein Deficiency Deafness, Autosomal Recessive 59 Deafness-Hypogonadism Syndrome Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Deafness, X-Linked 5 Delusional Disorder Dementia Demyelinating Disease Demyelinating Polyneuropathy Dengue Hemorrhagic Fever Dermatitis Dermatitis Herpetiformis, Familial Dermatomyositis De Sanctis-Cacchione Syndrome Desbuquois Dysplasia 1 Diabetes Mellitus Diabetes Mellitus, Noninsulin-Dependent Diabetic Angiopathy Diabetic Autonomic Neuropathy Diabetic Cataract Diabetic Foot Ulcers Diabetic Macular Edema Diabetic Mastopathy Diabetic Neuropathy Diabetic Polyneuropathy Diarrhea Diffuse Cutaneous Systemic Sclerosis Diffuse Infiltrative Lymphocytosis Syndrome Diffuse Large B-Cell Lymphoma Dilated Cardiomyopathy Diphtheria Distal Hereditary Motor Neuropathies Distal Hereditary Motor Neuropathy, Type Ii Distal Hereditary Motor Neuropathy, Type V Dnm2-Related Intermediate Charcot-Marie-Tooth Neuropathy Dnmt1-Related Dementia, Deafness, and Sensory Neuropathy Donnai-Barrow Syndrome Dry Eye Syndrome Duane Retraction Syndrome 1 Duodenitis Dysautonomia Dysentery Dyskeratosis Congenita Dyskinesia of Esophagus Dyslexia Dyspepsia Dysphagia Dystonia Eales Disease Eczema Herpeticum Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome, Hypermobility Type Elephantiasis Empty Sella Syndrome Encephalitis Encephalomyopathy Encephalopathy Endemic Typhus Endocarditis Endometriosis Endotheliitis End Stage Renal Failure Engraftment Syndrome Enterocolitis Enteropathica Enthesopathy Eosinophilia-Myalgia Syndrome Eosinophilic Fasciitis Eosinophilic Granulomatosis with Polyangiitis Epicondylitis Epidermolysis Bullosa Epidural Abscess Epilepsy Epileptic Encephalopathy, Early Infantile, 6 Epithelial Recurrent Erosion Dystrophy Erythema Elevatum Diutinum Erythermalgia, Primary Erythroderma, Ichthyosiform, Congenital Reticular Erythromelalgia Ethylene Glycol Poisoning Exocrine Pancreatic Insufficiency Exophthalmos Exostosis Fabry Disease Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature Facial Paralysis Facial Spasm Familial Adenomatous Polyposis 1 Familial Amyloidosis, Finnish Type Familial Glucocorticoid Deficiency Fanconi Anemia, Complementation Group E Fasciitis Fazio-Londe Disease Fecal Incontinence Feingold Syndrome 1 Femoral Neuropathy Fibrocalculous Pancreatopathy Fibrosarcoma Fibrous Dysplasia Focal Dystonia Focal Segmental Glomerulosclerosis Foot Drop Foster-Kennedy Syndrome Fragile X-Associated Tremor/ataxia Syndrome Galactose Epimerase Deficiency Galactosemia Galactosialidosis Gars-Associated Axonal Neuropathy Gastric Dilatation Gastric Lymphoma Gastroesophageal Reflux Gastrointestinal Stromal Tumor Gastroparesis Genetic Prion Diseases Gestational Diabetes Gianotti Crosti Syndrome Giant Axonal Neuropathy Giant Cell Tumor Gigantism Gilles De La Tourette Syndrome Gingivitis Gitelman Syndrome Glaucoma, Hereditary Glaucoma-Related Pigment Dispersion Syndrome Glaucomatocyclitic Crisis Glioma Glomerulonephritis Glomus Tumor Glossodynia Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency Glucose Transporter Type 1 Deficiency Syndrome Glycogen Storage Disease Goiter Goldberg-Shprintzen Syndrome Gonadal Dysgenesis Gordon Holmes Syndrome Gout Graft-Versus-Host Disease Granulomatous Angiitis Granulomatous Hypophysitis Graves' Disease Growth Hormone Deficiency Guillain-Barre Syndrome Guillain-Barre Syndrome, Familial Hajdu-Cheney Syndrome Handl Syndrome Hansen's Disease Harlequin Syndrome Hashimoto Thyroiditis Headache Heavy Chain Deposition Disease Helicobacter Pylori Infection Helix Syndrome Hellp Syndrome Hemangioma Hemangioma-Thrombocytopenia Syndrome Hematopoietic Stem Cell Transplantation Hemolytic Anemia Hemolytic Anemia, Cd59-Mediated, with or Without Immune-Mediated Polyneuropathy Hemophagocytic Lymphohistiocytosis Hemophilia Hemorrhagic Fever Hemosiderosis Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis E Hereditary Amyloidosis Hereditary Ataxia Hereditary Motor and Sensory Neuropathy, Type Iic Hereditary Multiple Exostoses Hereditary Neuropathies Hereditary Neuropathy with Liability to Pressure Palsy Hereditary Sensory and Autonomic Neuropathy Type 1e Hereditary Sensory Neuropathy Hereditary Spastic Paraplegia Hereditary Spherocytosis Herpes Simplex Herpes Zoster Herpes Zoster Ophthalmicus Herpetic Whitlow Hidradenitis Hidradenitis Suppurativa Homocystinuria Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis Human Coronavirus Sensitivity Huntington Disease Hydrolethalus Syndrome 1 Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperacusis Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant Hypereosinophilic Syndrome Hyperglycemia Hyperhidrosis, Gustatory Hyperinsulinism Hypermobility Syndrome Hyperostosis Hyperreflexia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Retinopathy Hypertrichosis Hypertrophic Neuropathy of Dejerine-Sottas Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertrophic Pyloric Stenosis Hypoaldosteronism Hypoascorbemia Hypoglycemia Hypogonadism Hypogonadotropic Hypogonadism 1 with or Without Anosmia Hypohidrosis Hypokalemia Hypomelanotic Disorder Hypomyelinating Leukodystrophy Hypoparathyroidism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatemia Hyporeninemic Hypoaldosteronism Hypotonia Hypoxia Ichthyosis Idiopathic Inflammatory Myopathy Igg4-Related Disease Igg4-Related Pachymeningitis Immune-Complex Glomerulonephritis Immunoglobulin E Concentration, Serum Impotence Inappropriate Adh Syndrome Inclusion Body Myositis Infantile Axonal Neuropathy Infertility Inflammatory Bowel Disease Inflammatory Bowel Disease 1 Influenza Infundibulo-Neurohypophysitis Inherited Metabolic Disorder Insensitivity to Pain, Congenital, with Anhidrosis Insulin-Like Growth Factor I Insulinoma Internuclear Ophthalmoplegia Interstitial Nephritis Intestinal Perforation Intestinal Pseudo-Obstruction Intracranial Aneurysm Intracranial Hypertension Intracranial Hypotension Intraneural Perineurioma Iritis Ischemia Ischemic Colitis Ischemic Neuropathy Ischemic Optic Neuropathy Isoniazid Toxicity Jackson-Weiss Syndrome Juvenile Glaucoma Kabuki Syndrome 1 Kagami-Ogata Syndrome Kaufman Oculocerebrofacial Syndrome Kearns-Sayre Syndrome Keratoconus Krabbe Disease Lactic Acidosis Lambert-Eaton Myasthenic Syndrome Large Granular Lymphocyte Leukemia Laryngeal Abductor Paralysis Laryngeal Cleft Laryngitis Lateral Sclerosis Lathyrism Lattice Corneal Dystrophy Laurence-Moon Syndrome Leber Hereditary Optic Neuropathy Leber Optic Atrophy Leber Optic Atrophy and Dystonia Legius Syndrome Leigh Syndrome Leiomyoma Lentigines Leopard Syndrome Lepromatous Leprosy Leukemia Leukodystrophy Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lewis-Sumner Syndrome Light and Heavy Chain Deposition Disease Light Chain Deposition Disease Limb-Girdle Muscular Dystrophy Limbic Encephalitis Limb Ischemia Lipodystrophy Lipodystrophy, Congenital Generalized, Type 2 Lipomatosis Lipomatosis, Multiple Lissencephaly Lissencephaly 1 Littoral Cell Angioma of the Spleen Livedoid Vasculopathy Liver Cirrhosis Liver Disease Localized Hypertrophic Neuropathy Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Low Tension Glaucoma Lung Cancer Lung Disease Lupus Erythematosus Lyme Disease Lymphedema Lymphoblastic Leukemia Lymphoma Lymphomatoid Granulomatosis Lymphomatous Meningitis Lymphosarcoma Machado-Joseph Disease Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Macrocytic Anemia Macroglobulinemia Macrophage Activation Syndrome Macular Holes Majeed Syndrome Malignant Hypertension Malignant Peripheral Nerve Sheath Tumor Mannosidosis, Beta a, Lysosomal Maple Syrup Urine Disease Marek Disease Mccune-Albright Syndrome Mcleod Syndrome Median Neuropathy Mediastinal Cancer Mediastinitis Megacolon Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 Megalencephaly Melanoma Membranoproliferative Glomerulonephritis Membranous Nephropathy Meningioma, Familial Meningitis Meningococcemia Meningoencephalitis Meralgia Paresthetica Metachromatic Leukodystrophy Metatropic Dysplasia Methemoglobinemia Methylmalonic Aciduria and Homocystinuria, Cblc Type Microcephaly Microscopic Polyangiitis Microvascular Complications of Diabetes 1 Migraine with Aura Miliary Tuberculosis Miller Fisher Syndrome Mitochondrial Disorders Mitochondrial Dna-Associated Leigh Syndrome and Narp Mitochondrial Dna Depletion Syndrome 7 Mitochondrial Encephalomyopathy Mitochondrial Myopathy Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Mitochondrial Trifunctional Protein Deficiency Mixed Connective Tissue Disease Moebius Syndrome Monoclonal Paraproteinemia Mononeuritis Multiplex Mononeuropathy Mononeuropathy of the Median Nerve, Mild Morbid Obesity Motor Neuron Disease Motor Peripheral Neuropathy Mucolipidosis Iii Alpha/beta Mucopolysaccharidosis, Type Vii Mucositis Multifocal Choroiditis Multifocal Motor Neuropathy Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Multiple Acyl-Coa Dehydrogenase Deficiency Multiple Cranial Nerve Palsy Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Multiple Self-Healing Squamous Epithelioma Multiple Symmetrical Lipomatosis Muscle Hypertrophy Muscular Atrophy Muscular Dystrophy Musical Perfect Pitch Myasthenia Gravis Myelitis Myelodysplastic Syndrome Myeloid Leukemia Myeloma, Multiple Myocardial Infarction Myoclonus Myoclonus Epilepsy Myofascial Pain Syndrome Myofibrillar Myopathy Myoma Myopathy Myositis Myositis Ossificans Myotonic Dystrophy Natural Killer Cell Leukemia Necrotizing Fasciitis Neovascular Glaucoma Nerve Compression Syndrome Nervous System Disease Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neuritis Neuroaxonal Dystrophy Neuroblastoma Neuroendocrine Tumor Neurofibroma Neurofibromatosis, Type Iv, of Riccardi Neurofibrosarcoma Neurogenic Arthropathy Neurogenic Bladder Neuroleptic Malignant Syndrome Neuroma Neuromuscular Disease Neuromyelitis Optica Neuromyotonia and Axonal Neuropathy, Autosomal Recessive Neuronal Intranuclear Inclusion Disease Neuronitis Neuropathy, Ataxia, and Retinitis Pigmentosa Neuropathy, Congenital Hypomyelinating or Amyelinating, Autosomal Recessive Neuropathy, Hereditary Motor and Sensory, Russe Type Neuropathy, Hereditary Motor and Sensory, Type Via Neuropathy, Hereditary Sensory and Autonomic, Type Ia Neuropathy, Hereditary Sensory and Autonomic, Type Iia Neuropathy, Hereditary Sensory and Autonomic, Type Iii Neuropathy, Hereditary Sensory and Autonomic, Type V Neuropathy, Hereditary Sensory and Autonomic, Type Vii Neuropathy, Hereditary Sensory and Autonomic, Type Viii Neuropathy, Hereditary Sensory, Type Ie Neuropathy, Hereditary Thermosensitive Neuropathy, Hereditary, with Liability to Pressure Palsies Neuropathy, Painful Neuroretinitis Neurosarcoidosis Neurosyphilis Neurotrophic Keratopathy Neutropenia Neutrophilic Dermatosis, Acute Febrile Nevus Comedonicus Niemann-Pick Disease Night Blindness Nodular Regenerative Hyperplasia Nonarteritic Anterior Ischemic Optic Neuropathy Noonan Syndrome with Multiple Lentigines Notalgia Paresthetica Nutritional Optic Neuropathy Occipital Horn Syndrome Ocular Hypertension Oculopharyngeal Muscular Dystrophy Odontoma Olecranon Bursitis Olivopontocerebellar Atrophy Open-Angle Glaucoma Optic Atrophy 1 Optic Atrophy 3, Autosomal Dominant Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy Optic Disk Drusen Optic Nerve Disease Optic Nerve Hypoplasia, Bilateral Optic Nerve Sheath Meningioma Optic Neuritis Orbital Cellulitis Orbital Varix Orthostatic Intolerance Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteochondroma Osteomalacia Osteomyelitis Osteonecrosis Osteopetrosis Osteosclerotic Myeloma Ovarian Cancer Overhydrated Hereditary Stomatocytosis Paine Syndrome Pancreatic Cancer Pancreatitis Pancytopenia Panuveitis Papilledema Papular Mucinosis Paramyloidosis Paraplegia Parkinson Disease 15, Autosomal Recessive Early-Onset Parkinson Disease 2, Autosomal Recessive Juvenile Parkinson Disease 6, Autosomal Recessive Early-Onset Parsonage Turner Syndrome Pdgfrb-Associated Chronic Eosinophilic Leukemia Pediatric Systemic Lupus Erythematosus Pelizaeus-Merzbacher Disease Pellagra Pemphigus Pemphigus Foliaceus Perineurioma Periostitis Peripheral Artery Disease Peripheral Nervous System Disease Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss Peritonitis Pernicious Anemia Peroneal Nerve, Accessory Deep Peroneal Nerve Paralysis Peroneal Neuropathy Perrault Syndrome Persistent Idiopathic Facial Pain Pertussis Petrositis Pfeiffer Syndrome Phaeochromocytoma Pharyngitis Pheochromocytoma Pick Disease of Brain Pigmented Villonodular Synovitis Pilocytic Astrocytoma Pituitary Adenoma Pituitary Apoplexy Plantar Fasciitis Plasma Cell Neoplasm Plasmacytoma Plexopathy Pneumonia Poems Syndrome Polyarteritis Nodosa Polycythemia Polycythemia Vera Polykaryocytosis Inducer Polymicrogyria Polyneuropathy Polyneuropathy Associated with Igm Monoclonal Gammapathy with Anti-Mag Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes Polyradiculoneuropathy Polyradiculopathy Pontine Hemorrhage Pontine Tegmental Cap Dysplasia Pontocerebellar Hypoplasia Popliteal Cyst Porphyria Porphyria, Acute Intermittent Posner-Schlossman Syndrome Posterior Column Ataxia Posterior Column Ataxia with Retinitis Pigmentosa Postherpetic Neuralgia Postural Hypotension Prediabetes Syndrome Premature Chromatid Separation Trait Primary Angiitis of the Central Nervous System Primary Angle-Closure Glaucoma Primary Cerebellar Degeneration Primary Hyperoxaluria Primary Orthostatic Hypotension Prion Disease 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 Propionic Acidemia Prostatitis Protein S Deficiency Proteus Syndrome Prurigo Nodularis Pseudomyotonia Pseudomyxoma Peritonei Pseudoxanthoma Elasticum Psoriasis Psoriasis 13 Psoriatic Arthritis Ptosis Pulmonary Alveolar Microlithiasis Pulmonary Edema Pulmonary Hypertension Pulmonary Sarcoidosis Punctate Inner Choroidopathy Pure Mitochondrial Myopathy Purpura Pustulosis Palmaris Et Plantaris Pyloric Stenosis Pyridoxine Deficiency Quadriplegia Rabies Radial Nerve Lesion Radial Neuropathy Radiculopathy Rapidly Progressive Glomerulonephritis Recessive Dystrophic Epidermolysis Bullosa Reflex Sympathetic Dystrophy Refractive Error Refsum Disease, Classic Relapsing Fever Relapsing Polychondritis Renal Osteodystrophy Renal Tuberculosis Renpenning Syndrome 1 Resting Heart Rate, Variation in Restless Legs Syndrome Retinal Artery Occlusion Retinal Degeneration Retinal Detachment Retinal Vascular Occlusion Retinal Vasculitis Retinal Vein Occlusion Retinitis Retinitis Pigmentosa Rheumatic Disease Rheumatoid Arthritis Riboflavin Deficiency Riboflavin Transporter Deficiency Neuronopathy Richards-Rundle Syndrome Robinow Syndrome, Autosomal Recessive Rocky Mountain Spotted Fever Rosai-Dorfman Disease Roussy-Levy Hereditary Areflexic Dystasia Sacral Plexopathy Salt and Pepper Developmental Regression Syndrome Sandhoff Disease Sarcoidosis 2 Sarcoma Satb2-Associated Syndrome Sciatic Neuropathy Scleritis Scrub Typhus Sebastian Syndrome Seizures, Benign Familial Neonatal, 1 Seminoma Sensorineural Hearing Loss Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis Sensory Neuropathy Type 1 Sensory Peripheral Neuropathy Septic Arthritis Serotonin Syndrome Severe Infantile Axonal Neuropathy Short Stature, Developmental Delay, and Congenital Heart Defects Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sialolithiasis Sick Building Syndrome Sickle Cell Disease Siderosis Silent Myocardial Infarction Sinonasal Undifferentiated Carcinoma Skeletal Dysplasias Skin Sarcoidosis Skull Base Meningioma Sleep Apnea Sleep Disorder Small Cell Carcinoma Smith-Kingsmore Syndrome Smith-Magenis Syndrome Soft Tissue Sarcoma Spastic Ataxia Spastic Ataxia, Charlevoix-Saguenay Type Spastic Cerebral Palsy Spasticity Spastic Paraparesis Spastic Paraplegia 30, Autosomal Recessive Spastic Paraplegia 3a Spastic Paraplegia 55, Autosomal Recessive Spastic Paraplegia 57, Autosomal Recessive Spastic Paraplegia, Optic Atrophy, and Neuropathy Spinal Cord Disease Spinal Cord Infarction Spinal Cord Injury Spinal Muscular Atrophy Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1 Spinal Muscular Atrophy, Distal, X-Linked 3 Spinocerebellar Ataxia 18 Spinocerebellar Ataxia 25 Spinocerebellar Ataxia 4 Spinocerebellar Ataxia 43 Spinocerebellar Ataxia Type 1 with Axonal Neuropathy Spinocerebellar Degeneration Spondylitis Spondyloarthropathy 1 Spondyloocular Syndrome Spondylosis Spontaneous Intracranial Hypotension Spotted Fever Squamous Cell Carcinoma Status Asthmaticus Status Epilepticus Steatorrhea Stiff-Person Syndrome Strabismus Streptococcal Toxic-Shock Syndrome Sturge-Weber Syndrome Subacute Cutaneous Lupus Erythematosus Substance Abuse Substernal Goiter Superior Mesenteric Artery Syndrome Suppressor of Tumorigenicity 3 Susac Syndrome Sveinsson Chorioretinal Atrophy Swine Influenza Syncope Syndrome of Inappropriate Antidiuretic Hormone Synostosis Synovitis Syphilis Syphilitic Myelopathy Syringomyelia Systemic Lupus Erythematosus Systemic Mastocytosis Tabes Dorsalis Takayasu Arteritis Talipes Equinovarus Tangier Disease Tarlov Cysts Tarsal Tunnel Syndrome Tay-Sachs Disease T-Cell Large Granular Lymphocyte Leukemia T-Cell Leukemia Temple-Baraitser Syndrome Temporal Arteritis Temporal Lobe Epilepsy Tendinitis Testicular Seminoma Tetanus Tethered Cord Syndrome Thoracic Outlet Syndrome Thrombocytopenia Thrombocytosis Thrombophilia Thrombophlebitis Thrombosis Thymoma Thyroiditis Tibia, Hypoplasia or Aplasia of, with Polydactyly Tibial Neuropathy Tick Paralysis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Tolosa-Hunt Syndrome Tooth Disease Torticollis Townes-Brocks Syndrome Toxic Oil Syndrome Toxic Optic Neuropathy Toxic Shock Syndrome Tracheitis Transsexualism Transsexuality Transverse Myelitis Traumatic Brain Injury Tremor Trichohepatoenteric Syndrome 1 Trigeminal Neuralgia Triosephosphate Isomerase Deficiency Trisomy 17 Mosaicism Tropical Spastic Paraparesis Tuberculoid Leprosy Tuberculum Sellae Meningioma Tumor Suppressor Gene on Chromosome 11 Turner Syndrome Type Ii Mixed Cryoglobulinemia Tyrosinemia Ulcerative Colitis Ulnar Nerve Lesion Ulnar Neuropathy Uremia Uremic Neuropathy Urethral Stricture Urethritis Usher Syndrome Uterine Anomalies Uterine Corpus Cancer Uveitis Vaginitis Varicose Veins Vascular Disease Vasculitis Vestibular Disease Vestibular Neuronitis Villonodular Synovitis Vitamin B12 Deficiency Vitreoretinal Degeneration Vitreoretinal Dystrophy Vitreous Detachment Vogt-Koyanagi-Harada Disease Waardenburg Syndrome Type 4 Waldenstrom Macroglobulinemia Wallerian Degeneration Warburg Micro Syndrome Weber Syndrome Wernicke Encephalopathy Wernicke-Korsakoff Syndrome West Syndrome Whipple Disease Wild Type Attr Amyloidosis Wilson Disease Wolff-Parkinson-White Syndrome Wolfram Syndrome Wrinkles Xanthomatosis Yemenite Deaf-Blind Hypopigmentation Syndrome Zika Virus Infection