Skip to main content
EUTOPIA
SCHOOL
CUNOAȘTERE și AUTOCUNOAȘTERE
caută sub nivelul curent
caută în tot site-ul
Search
Începeţi acum
Login
Continuă cu:
Sunt de acord cu
termenii şi condiţii
Sunt de acord cu
primirea de materiale de marketing
ÎNREGISTRARE
»
Cumpărător - persoană fizică
Cumpărător - companie
Distribuitor
Close
»
Eutopia e-LEARNING
»
ȘTIINȚE APLICATE
»
Ramuri ale științelor aplicate
»
Știința sănătății
»
Boli, Tulburări & Simptome
»
XX Boli-semne, simptome
»
Neuronitis
Informaţii despre
Nume
Neuronitis
Pagina Web
www.malacards.org
Clasificare anatomică Malacards
Boli neuronale
Vezi şi
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
Please wait...