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Nume Cerebritis
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Boli A-Z 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 3-Methylcrotonyl-Coa Carboxylase Deficiency 3-Methylglutaconic Aciduria Aarskog-Scott Syndrome Abdominal Tuberculosis Abducens Nerve Disease Abducens Palsy Ablepharon-Macrostomia Syndrome Absence of Septum Pellucidum Aceruloplasminemia Achalasia Achromatopsia Acoustic Neuroma Acquired Hemophilia Acquired Hemophilia a Acquired Immunodeficiency Syndrome Acrocallosal Syndrome Acrodermatitis Acromegaly Actinomycosis Acute Chest Syndrome Acute Diarrhea Acute Disseminated Encephalomyelitis Acute Insulin Response Acute Leukemia Acute Liver Failure Acute Lymphoblastic Leukemia, Childhood Acute Lymphocytic Leukemia Acute Motor Axonal Neuropathy Acute Mountain Sickness Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Acute Myocardial Infarction Acute Myocarditis Acute Necrotizing Encephalopathy Acute Pancreatitis Acute Porphyria Acute Posterior Multifocal Placoid Pigment Epitheliopathy Acute Poststreptococcal Glomerulonephritis Acute Promyelocytic Leukemia Acute Respiratory Distress Syndrome Acute Stress Disorder Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of Adams-Oliver Syndrome Adenocarcinoma Adenoiditis Adenoma Adenomyosis Adenosine Deaminase 2 Deficiency Adenosine Deaminase Deficiency Adiponectin, Serum Level of, Quantitative Trait Locus 1 Adrenoleukodystrophy Adrenomyeloneuropathy Adult Respiratory Distress Syndrome Afibrinogenemia Agammaglobulinemia Aganglionosis, Total Intestinal Aging Agnosia Agoraphobia Agraphia Aicardi-Goutieres Syndrome Aids Dementia Complex Akinetic Mutism Akinetopsia Alagille Syndrome 1 Aland Island Eye Disease Albinism-Deafness Syndrome Alcohol Abuse Alcohol Dependence Alcohol-Related Neurodevelopmental Disorder Alexander Disease Alexia Allergic Bronchopulmonary Aspergillosis Allergic Bronchopulmonary Aspergillosis, Familial Alopecia 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 Alpha-Thalassemia Alport Syndrome, X-Linked Al-Raqad Syndrome Alternating Hemiplegia of Childhood Alveolar Echinococcosis Alveolar Soft Part Sarcoma Alzheimer Disease 19 Alzheimer Disease 3 Amaurosis Fugax Amebiasis Amphetamine Abuse Amusia Amyloidosis Amyloidosis, Primary Localized Cutaneous, 1 Amyotonia Congenita Anal Squamous Cell Carcinoma Anaplastic Ependymoma Anaplastic Ganglioglioma Anaplastic Large Cell Lymphoma Anaplastic Oligodendroglioma Anauxetic Dysplasia 1 Anca-Associated Vasculitis Ancylostomiasis Androgen Insensitivity, Partial Androgen Insensitivity Syndrome Anencephaly Aneurysm Angelman Syndrome Angina Pectoris Angiocentric Glioma Angiodysplasia Angioedema Angioimmunoblastic T-Cell Lymphoma Angiokeratoma Angiomatosis Angiosarcoma Angiosarcoma of the Scalp Aniridia 1 Anisocoria Anisometropia Ankylosis Anorexia Nervosa 1 Anosmia Anosognosia Anoxia Anterior Cerebral Artery Infarction Anterograde Amnesia Antiphospholipid Syndrome Antithrombin Iii Deficiency Anuria Aortic Aneurysm Aortic Arch Interruption Aortic Atherosclerosis Aortic Coarctation Aortic Disease Aortic Valve Disease 2 Aortic Valve Insufficiency Aortitis Aphasia Aplastic Anemia Apnea, Obstructive Sleep Apparent Mineralocorticoid Excess Apraxia Arachnoid Cysts Arachnoiditis Argininemia Argyria Arterial Thoracic Outlet Syndrome Arteries, Anomalies of Arteriolosclerosis Arteriosclerosis Arteriosclerosis Obliterans Arteriovenous Fistula Arteriovenous Malformation Arteriovenous Malformations of the Brain Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 2a Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Aseptic Meningitis Asperger Syndrome Aspergillosis Asphyxia Neonatorum Aspiration Pneumonia Asplenia, Isolated Congenital Asthenopia Asthma Astroblastoma 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-Telangiectasia Athetosis Atlantoaxial Subluxation Atrial Fibrillation Atrial Septal Aneurysm Atrial Standstill Atrioventricular Block Atrioventricular Septal Defect Attention Deficit-Hyperactivity Disorder Atypical Teratoid Rhabdoid Tumor Audiogenic Seizures Aural Atresia, Congenital Autism Autism Spectrum Disorder Autoimmune Encephalitis Autoimmune Enteropathy Autoimmune Hepatitis Autoimmune Inner Ear Disease Autoimmune Lymphoproliferative Syndrome, Type V Autonomic Dysfunction Autonomic Neuropathy Autosomal Dominant Polycystic Kidney Disease Axonal Neuropathy Babesiosis Back Pain Bacterial Meningitis Baroreflex Failure Basaloid Follicular Hamartoma Basilar Artery Occlusion Basosquamous Carcinoma B-Cell Lymphomas Behr Syndrome Benign Adult Familial Myoclonic Epilepsy Benign Meningioma Beriberi Beta-Adrenergic Stimulation, Response to Beta-Thalassemia Bilateral Massive Adrenal Hemorrhage Binswanger's Disease Biotinidase Deficiency Bipolar Disorder Bipolar I Disorder Bladder Cancer Blastoma Blastomycosis Bleeding Disorder, Platelet-Type, 11 Blepharospasm Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Group, Junior System Blood Group--Kidd System Blue Rubber Bleb Nevus Body Dysmorphic Disorder 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 Bone Marrow Necrosis Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Borderline Personality Disorder Bornholm Eye Disease Brachydactyly Brachydactyly, Type E1 Brain Cancer Brain Compression Brain Edema Brain Germinoma Brain Glioma Brain Injury Brain Ischemia Brain Small Vessel Disease with or Without Ocular Anomalies Brainstem Auditory Evoked Responses Brain Stem Infarction Branchiootic Syndrome 1 Branch Retinal Artery Occlusion Breast Cancer Brittle Bone Disorder Bronchogenic Cyst Bronchopneumonia Bronchopulmonary Dysplasia Brugada Syndrome Bruxism Budd-Chiari Syndrome Buerger Disease Burning Mouth Syndrome Burns Bursitis C1q Deficiency Calcinosis Calciphylaxis Canavan Disease Candidiasis Cannabis Dependence Capgras Syndrome Capillary Leak Syndrome Capillary Malformation-Arteriovenous Malformation Cardiac Arrest Cardiac Rupture Cardiac Tamponade Cardiogenic Shock Carney Complex Variant Carotid Artery Disease Carotid Artery Dissection Carotid Artery Occlusion Carotid Artery Thrombosis Carotid Stenosis Carpal Tunnel Syndrome Castleman Disease Cataract Cataract 5, Multiple Types Catastrophic Antiphospholipid Syndrome Cat-Scratch Disease Cavernous Hemangioma Cavernous Malformation Cavernous Sinus Thrombosis Cavitary Optic Disc Anomalies Cellulitis Central Nervous System Disease Central Nervous System Germinoma Central Nervous System Lymphoma Central Nervous System Origin Vertigo Central Nervous System Tuberculosis Central Nervous System Vasculitis Central Neurocytoma Centralopathic Epilepsy Central Pontine Myelinolysis Central Precocious Puberty Central Retinal Artery Occlusion Central Sleep Apnea Cerebellar Degeneration Cerebellar Disease Cerebellar Hypoplasia Cerebellar Medulloblastoma Cerebellofaciodental Syndrome Cerebral Amyloid Angiopathy, App-Related Cerebral Amyloid Angiopathy, Cst3-Related Cerebral Amyloid Angiopathy, Itm2b-Related, 1 Cerebral Amyloid Angiopathy, Itm2b-Related, 2 Cerebral Aneurysms Cerebral Angioma Cerebral Arterial Disease Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 Cerebral Arteriopathy, Autosomal Recessive, with Subcortical Infarcts and Leukoencephalopathy Cerebral Arteriosclerosis Cerebral Arteritis Cerebral Artery Occlusion Cerebral Atherosclerosis Cerebral Atrophy Cerebral Beriberi Cerebral Cavernous Malformation, Familial Cerebral Cavernous Malformations Cerebral Cavernous Malformations 2 Cerebral Cavernous Malformations 3 Cerebral Creatine Deficiency Syndrome Cerebral Creatine Deficiency Syndrome 1 Cerebral Degeneration Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome Cerebral Folate Deficiency Cerebral Hemorrhage Cerebral Hypoxia Cerebral Lipidosis Cerebral Lymphoma Cerebral Meningioma Cerebral Neuroblastoma Cerebral Palsy Cerebral Palsy, Ataxic, Autosomal Recessive Cerebral Primitive Neuroectodermal Tumor Cerebral Sarcoidosis Cerebral Sarcoma Cerebral Sinovenous Thrombosis Cerebral Visual Impairment Cerebrocostomandibular Syndrome Cerebroretinal Microangiopathy with Calcifications and Cysts 1 Cerebrospinal Fluid Leak Cerebrotendinous Xanthomatosis Cerebrovascular Disease Ceroid Lipofuscinosis, Neuronal, 6 Cervical Dystonia Cervical Rib Cervicitis Chagas Disease Chanarin-Dorfman Syndrome Charcot-Marie-Tooth Disease Charles Bonnet Syndrome Chiari Malformation Chiasmal Syndrome Chickenpox Childhood Leukemia Childhood Medulloblastoma Childhood-Onset Cerebral X-Linked Adrenoleukodystrophy Childhood-Onset Schizophrenia Chlamydia Choanal Atresia, Posterior Cholangiocarcinoma Cholangitis Cholera Cholesteatoma Cholesterol Embolism Chondroblastoma Chondrodysplasia Punctata Syndrome Chondroma Chondrosarcoma Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction Chorioamnionitis Chorioangioma Choriocarcinoma Chorioretinitis Choroideremia Choroiditis Choroid Plexus Cyst Chromoblastomycosis Chromophobe Adenoma Chromosomal Triplication Chromosome 16 Trisomy Chronic Fatigue Syndrome Chronic Graft Versus Host Disease Chronic Granulomatous Disease Chronic Inflammatory Demyelinating Polyradiculoneuropathy Chronic Meningitis Chronic Mountain Sickness Chronic Mucocutaneous Candidiasis Chronic Neutrophilic Leukemia Chronic Pain Chronic Thromboembolic Pulmonary Hypertension Churg-Strauss Syndrome Citrullinemia, Classic Classic Phenylketonuria Cleft Larynx, Posterior Cleft Lip Clopidogrel Resistance Clubfoot Cluster Headache Cluttering Cocaine Abuse Cocaine Dependence Coccidioidomycosis Cockayne Syndrome Codas Syndrome Coenurosis Coffin-Lowry Syndrome Colitis Collagenous Colitis Colonic Pseudo-Obstruction Color Blindness Colorectal Cancer Common Cold Common Variable Immunodeficiency Communicating Hydrocephalus Compartment Syndrome Complement Factor B Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complex Partial Epilepsy Complex Regional Pain Syndrome Congenital Bile Acid Synthesis Defect Congenital Communicating Hydrocephalus Congenital Contractures Congenital Cystic Eye Congenital Cytomegalovirus Congenital Dyserythropoietic Anemia Congenital Hepatic Fibrosis Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi Congenital Methemoglobinemia Congenital Portosystemic Shunt Congenital Rubella Congenital Toxoplasmosis Congenital Zika Syndrome Congestive Heart Failure Conjunctivitis Constipation Constricting Bands, Congenital Conversion Disorder Coproporphyria, Hereditary Corneal Dystrophy, Fleck Coronary Artery Aneurysm Coronary Stenosis Coronary Thrombosis Cortical Blindness Cortical Deafness Corticobasal Degeneration Cough Headache Cranial Meningocele Cranial Nerve Palsy Cranioectodermal Dysplasia 1 Craniofacial-Deafness-Hand Syndrome Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Craniopharyngioma Craniosynostosis Craniosynostosis 1 Creatine Deficiency Syndromes Crest Syndrome Creutzfeldt-Jakob Disease Crohn's Colitis Crohn's Disease Cryoglobulinemia Cryptococcal Meningitis Cryptococcosis Cutaneous Anthrax Cutaneous Mastocytosis Cutaneous T Cell Lymphoma Cutis Laxa Cutis Laxa, Autosomal Recessive, Type Iiia Cutis Marmorata Telangiectatica Congenita Cyanosis, Transient Neonatal Cyclic Vomiting Syndrome Cystic Echinococcosis Cysticercosis Cystic Fibrosis Cystinosis Cytomegalic Inclusion Disease Cytomegalovirus Infection D-2-Hydroxyglutaric Aciduria 1 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Deafness with Labyrinthine Aplasia Microtia and Microdontia Delusional Disorder Dementia Dementia Pugilistica Demyelinating Disease Dental Caries Dentatorubral-Pallidoluysian Atrophy Dermatitis Dermatomyositis Dermoid Cyst De Sanctis-Cacchione Syndrome Desmoplastic Infantile Ganglioglioma Developmental Coordination Disorder Developmental Dysplasia of the Hip 1 Dextrocardia Dextrocardia with Situs Inversus Diabetes Insipidus Diabetes Insipidus, Nephrogenic, Autosomal Diabetes Mellitus Diabetes Mellitus, Ketosis-Prone Diabetic Autonomic Neuropathy Diabetic Encephalopathy Diaphragmatic Hernia, Congenital Diarrhea Diastolic Heart Failure Diastrophic Dysplasia Diffuse Idiopathic Skeletal Hyperostosis Diffuse Large B-Cell Lymphoma Diffuse Lymphatic Malformation Digeorge Syndrome Dilated Cardiomyopathy Disseminated Intravascular Coagulation Distal Trisomy 3p Distomatosis Donnai-Barrow Syndrome Down Syndrome Drug Dependence Duane Retraction Syndrome 1 Duodenal Atresia Duodenal Obstruction Duodenitis Dural Sinus Malformation Dwarfism Dysautonomia Dyscalculia Dysgraphia Dyskinetic Cerebral Palsy Dyslexia Dysostosis Dyspepsia Dysphagia Dystonia Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency Earlobe Crease Early-Onset Generalized Limb-Onset Dystonia Early-Onset Schizophrenia Echinococcosis Echolalia Eclampsia Ectomesenchymoma Egg Allergy Ehrlichiosis Eisenmenger Syndrome Elliptocytosis 2 Empty Sella Syndrome Encephalitis Encephalitozoonosis Encephalocele Encephalocraniocutaneous Lipomatosis Encephalomalacia Encephalomyopathy Encephalopathy Endemic Goiter Endocarditis Endometrial Stromal Sarcoma Endophthalmitis Endotheliitis Enteropathica Eosinophilic Fasciitis Eosinophilic Granuloma Eosinophilic Granulomatosis with Polyangiitis Ependymoma Epidermoid Cysts Epidural Abscess Epignathus Epilepsy Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation Epileptic Encephalopathy, Early Infantile, 39 Epileptic Encephalopathy, Early Infantile, 6 Episodic Ataxia Epithelioid Hemangioendothelioma Epithelioid Sarcoma Erdheim-Chester Disease Erythermalgia, Primary Erythromelalgia Esophageal Atresia Esophageal Cancer Esotropia Essential Thrombocythemia Essential Tremor Ethanolaminosis Ethmoid Sinusitis Ethylene Glycol Poisoning Exhibitionism Exophthalmos Exotropia Extragonadal Germ Cell Cancer Extrapontine Myelinolysis Extrapulmonary Tuberculosis Extraventricular Neurocytoma Fabry Disease Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature Facial Hemiatrophy Factor Vii Deficiency Factor V Leiden Thrombophilia Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fainting Familial Chilblain Lupus Familial Hemiplegic Migraine Familial Tumoral Calcinosis Fanconi Anemia, Complementation Group E Fasciitis Fatal Familial Insomnia Febrile Seizures Fecal Incontinence Fetal Akinesia Deformation Sequence Fetal Alcohol Spectrum Disorder Fetal Alcohol Syndrome Fetishism Fibrocartilaginous Embolism Fibromuscular Dysplasia Fibrosarcoma Fibrous Dysplasia Fibrous Histiocytoma Floating-Harbor Syndrome Focal Dystonia Focal Epilepsy Foix Chavany Marie Syndrome Folate Malabsorption, Hereditary Folinic Acid-Responsive Seizures Fontaine Progeroid Syndrome Foot Drop Fragile X Syndrome Friedreich Ataxia 1 Frontal Sinusitis Frontometaphyseal Dysplasia Frontotemporal Dementia Frontotemporal Dementia, Chromosome 3-Linked Fumarase Deficiency Functional Diarrhea Galactose Epimerase Deficiency Galactosemia Gangliocytoma Ganglioglioma Ganglioneuroblastoma Gapo Syndrome Gardner-Diamond Syndrome Gastric Dilatation Gastroduodenitis Gastroesophageal Reflux Gastrointestinal Stromal Tumor Gastroschisis Gender Identity Disorder Generalized Anxiety Disorder Genetic Prion Diseases Germ Cells Tumors Gestational Choriocarcinoma Gestational Diabetes Gestational Diabetes Insipidus Giant Axonal Neuropathy Giant Cell Glioblastoma Gigantism Gilles De La Tourette Syndrome Gingival Overgrowth Gingivitis Glaucoma-Related Pigment Dispersion Syndrome Glioblastoma Glioblastoma Multiforme Glioma Gliomatosis Cerebri Gliosarcoma Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Glomerulonephritis Glossopharyngeal Neuralgia Glucose Intolerance Glutamyl Ribose-5-Phosphate Storage Disease Glutaric Acidemia I Glutathione Synthetase Deficiency Goiter Gonadal Dysgenesis Graft-Versus-Host Disease Granular Cell Tumor Granulocytopenia Granulomatous Amebic Encephalitis Granulomatous Angiitis Graves' Disease Griscelli Syndrome Growing Teratoma Syndrome Growth Control, Y-Chromosome Influenced Growth Hormone Deficiency Haim-Munk Syndrome Hair Disease Hairy Cell Leukemia Hall-Riggs Mental Retardation Syndrome Hall-Riggs Syndrome Hansen's Disease Hashimoto Thyroiditis Headache Headache Associated with Sexual Activity Head Injury Heart Sarcoma Helicobacter Pylori Infection Hellp Syndrome Hemangioblastoma Hemangioendothelioma Hemangioma Hemangiopericytoma, Malignant Hematopoietic Stem Cell Transplantation Hemicrania Continua Hemidystonia Hemifacial Atrophy, Progressive Hemifacial Spasm Hemihyperplasia, Isolated Hemimegalencephaly Hemiplegia Hemiplegic Migraine Hemoglobin E Disease Hemoglobinopathy Hemoglobinuria Hemolytic-Uremic Syndrome Hemopericardium Hemophagocytic Lymphohistiocytosis Hemophilia Hemophilia a Hemophilia B Hemorrhage, Intracerebral Hemorrhagic Shock and Encephalopathy Syndrome Hemosiderosis Hennekam Lymphangiectasia-Lymphedema Syndrome 1 Hennekam Syndrome Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Coma Hepatic Encephalopathy Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hepatoblastoma Hepatocellular Carcinoma Hepatorenal Syndrome Hereditary Angioedema Hereditary Ataxia Hereditary Cerebral Amyloid Angiopathy Hereditary Hemorrhagic Telangiectasia Hereditary Spastic Paraplegia Hereditary Spherocytosis Herpes Simplex Herpes Simplex Encephalitis Herpes Zoster Herpes Zoster Ophthalmicus Hinman Syndrome Hip Luxation Hip Subluxation Histiocytic Sarcoma Histiocytoma Histiocytosis Histoplasmosis Holocarboxylase Synthetase Deficiency Holoprosencephaly Holt-Oram Syndrome Homocysteinemia Homocystinuria Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Homozygous Familial Hypercholesterolemia Human Coronavirus Sensitivity Human Immunodeficiency Virus Type 1 Human Venous Malformation Huntington Disease Hurler Syndrome Hydranencephaly Hydrocephalus Hydronephrosis Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperacusis Hyperaldosteronism, Familial, Type I Hyperbilirubinemia, Rotor Type Hypercholesterolemia, Autosomal Dominant, 3 Hyperekplexia Hypereosinophilic Syndrome Hyperglycemia Hyper Ige Syndrome Hyperinsulinism Hyperlexia Hypermethioninemia Hyperostosis Hyperostosis Cranialis Interna Hyperostosis Frontalis Interna Hyperphenylalaninemia Hyperprolactinemia Hyperprolinemia Hypersomnia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hypertensive Heart Disease Hypertensive Nephropathy Hypertensive Retinopathy Hyperthyroidism Hypertonia Hypertrichosis Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertrophic Pyloric Stenosis Hypoadrenalism Hypoascorbemia Hypoglycemia Hypoglycemic Coma Hypomelanosis of Ito Hypoparathyroidism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypopituitarism Hypoplastic Left Heart Syndrome Hypothalamic Hamartomas Hypotonia Hypoxia Ichthyosis Ideomotor Apraxia Idiopathic Edema Idiopathic Hemiconvulsion-Hemiplegia Syndrome Idiopathic Hypersomnia Iminoglycinuria Immune Hydrops Fetalis Immune Suppression Immunodeficiency, Common Variable, 10 Immunoglobulin E Concentration, Serum Impotence Inappropriate Adh Syndrome Incontinentia Pigmenti Infantile Epileptic Encephalopathy Infantile Hypotonia Infantile Myofibromatosis Infective Endocarditis Inflammatory Bowel Disease Inflammatory Myofibroblastic Tumor Influenza Inherited Congenital Spastic Tetraplegia Inherited Metabolic Disorder Insulin-Like Growth Factor I Intellectual Disability - Athetosis - Microphthalmia Internuclear Ophthalmoplegia Interstitial Emphysema Intestinal Disease Intestinal Perforation Intracranial Aneurysm Intracranial Embolism Intracranial Hypertension Intracranial Hypotension Intracranial Sinus Thrombosis Intracranial Vasospasm Intraocular Lymphoma Intravascular Large B-Cell Lymphoma Intraventricular Meningioma Invasive Aspergillosis Invasive Mole Iron Deficiency Anemia Ischemia Ischemic Optic Neuropathy Ischemic Retinopathy Isolated Cleft Lip Isolated Growth Hormone Deficiency, Type Ia Japanese Encephalitis Juvenile Glaucoma Juvenile Rheumatoid Arthritis Juvenile Xanthogranuloma Kartagener Syndrome Kawasaki Disease Kearns-Sayre Syndrome Keratopathy Keratosis Keratosis Follicularis, Dwarfism, and Cerebral Atrophy Kernicterus Kleine-Levin Hibernation Syndrome Klippel-Trenaunay-Weber Syndrome Kluver-Bucy Syndrome Krabbe Disease Kuru Kwashiorkor Labyrinthitis Lactic Acidosis Landau-Kleffner Syndrome Langerhans Cell Histiocytosis Laryngitis Laryngomalacia Lateral Sclerosis Lateral Sinus Thrombosis Leiomyoma Leiomyosarcoma Lennox-Gastaut Syndrome Leopard Syndrome Lesch-Nyhan Syndrome Leukemia Leukodystrophy Leukodystrophy, Hypomyelinating, 6 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leukomalacia Leukostasis Light Chain Deposition Disease Limbic Encephalitis Linear Scleroderma Lipoid Proteinosis of Urbach and Wiethe Lipomatosis Liposarcoma Lissencephaly Lissencephaly 1 Listeriosis Livedoid Vasculopathy Liver Angiosarcoma Liver Cirrhosis Liver Disease Lobar Holoprosencephaly Locked-in Syndrome Loeffler Endocarditis Loeys-Dietz Syndrome Lupus Erythematosus Lyme Disease Lymphangioma Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphocytic Choriomeningitis Lymphocytic Hypophysitis Lymphocytic Vasculitis Lymphoma Lymphoma, Mucosa-Associated Lymphoid Type Lymphomatoid Granulomatosis Lymphopenia Lymphoplasmacytic Lymphoma Machado-Joseph Disease Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Macrophage Activation Syndrome Macrophagic Myofasciitis Macs Syndrome Major Affective Disorder 8 Major Affective Disorder 9 Malakoplakia Malaria Malignant Atrophic Papulosis Malignant Ectomesenchymoma Malignant Fibrous Histiocytoma of Bone Malignant Germ Cell Tumor Malignant Glioma Malignant Hypertension Malignant Hyperthermia Malignant Otitis Externa Malignant Peripheral Nerve Sheath Tumor Malignant Struma Ovarii Mannosidosis Maple Syrup Urine Disease Marantic Endocarditis Marasmus Marchiafava Bignami Disease Marfan Syndrome Mast Cell Activation Syndrome Mastoiditis Mature Teratoma Maxillary Sinusitis May-Hegglin Anomaly May-Thurner Syndrome Mcleod Syndrome Measles Median Arcuate Ligament Syndrome Medulloblastoma Medulloepithelioma Medullomyoblastoma Megakaryocytic Leukemia Megalencephaly Megaloblastic Anemia Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency Megalocornea Meier-Gorlin Syndrome 1 Melancholia Melanoma Melioidosis Melkersson-Rosenthal Syndrome Membranoproliferative Glomerulonephritis Membranous Nephropathy Meningeal Melanocytoma Meningioma, Familial Meningitis Meningitis and Encephalitis Meningocele Meningococcal Infection Meningococcal Meningitis Meningoencephalitis Menkes Disease Metabolic Acidosis Metachromatic Leukodystrophy Metal Allergy Methanol Poisoning Methemoglobinemia Methemoglobinemia, Beta-Globin Type Microcephaly Microcephaly, Epilepsy, and Diabetes Syndrome Microcystic Meningioma Microphthalmia Microscopic Polyangiitis Microsporidiosis Microtia Middle Cerebral Artery Infarction Middle Ear Disease Migraine with Aura Migraine with or Without Aura 1 Migraine Without Aura Miliary Tuberculosis Miller-Dieker Lissencephaly Syndrome Miller Fisher Syndrome Mills Syndrome Mitochondrial Disorders Mitochondrial Dna Depletion Syndrome 4a Mitochondrial Encephalomyopathy Mitochondrial Neurogastrointestinal Encephalomyopathy Mixed Cerebral Palsy Miyoshi Muscular Dystrophy 1 Moebius Syndrome Mollaret Meningitis Molybdenum Cofactor Deficiency Mononeuropathy Monosomy 22 Mood Disorder Morning Glory Syndrome Morphine Dependence Mosaic Trisomy 9 Motor Neuron Disease Movement Disease Moyamoya Disease 1 Mucinous Adenocarcinoma Mucolipidosis Iv Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Vii Mucositis Multidrug-Resistant Tuberculosis Multiple Chemical Sensitivity Multiple Cranial Nerve Palsy Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Multiple Sclerosis 3 Multiple System Atrophy 1 Multiple System Atrophy, Parkinsonian Type Mungan Syndrome Muscle Eye Brain Disease Muscular Atrophy Muscular Dystrophy Musical Perfect Pitch Mutism Myasthenia Gravis Mycetoma Mycobacterium Fortuitum Mycobacterium Kansasii Myelitis Myelodysplastic Syndrome Myeloid Leukemia Myelomeningocele Myeloproliferative Neoplasm Myiasis Myoblastoma Myocardial Infarction Myocardial Stunning Myocarditis Myoclonic Epilepsy of Lafora Myoclonus Myoma Myopathy Myositis Myositis Ossificans Myotonia Congenita, Autosomal Dominant Myotonic Dystrophy Myxofibrosarcoma Myxoma, Intracardiac Myxopapillary Ependymoma Myxosarcoma Narcolepsy Nasal Cavity Squamous Cell Carcinoma Nasal Encephalocele Natural Killer Cell Leukemia Necrobiotic Xanthogranuloma Necrotizing Fasciitis Neonatal Abstinence Syndrome Neonatal Anemia Neonatal Antiphospholipid Syndrome Neonatal Diabetes Mellitus Neonatal Herpes Neonatal Hypothyroidism Neonatal Jaundice Neonatal Meningitis Neonatal Stroke Neovascular Glaucoma Nephrosclerosis Nephrotic Syndrome Nervous System Disease Neu-Laxova Syndrome 1 Neuraminidase Deficiency Neurilemmoma Neuritis Neuroaxonal Dystrophy Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type I Neurofibromatosis, Type Iv, of Riccardi Neurofibrosarcoma Neurogenic Bladder Neurogenic Hypertension Neuroleptic Malignant Syndrome Neuroma Neuromyelitis Optica Neuromyelitis Optica Spectrum Disorder Neuronal Ceroid Lipofuscinosis Neuronal Migration Disorders Neuronitis Neuropathy Neurosarcoidosis Neuroschistosomiasis Neurosyphilis Neutropenia Neutrophil Actin Dysfunction Nevoid Hypermelanosis, Linear and Whorled Nevus Comedonicus Nevus, Epidermal Nevus of Ota Niemann-Pick Disease Nocardiosis Non-Involuting Congenital Hemangioma Non-Langerhans-Cell Histiocytosis Norrie Disease Obsessive-Compulsive Disorder Obstructive Hydrocephalus Obstructive Jaundice Ochronosis Ocular Motor Apraxia Ocular Toxoplasmosis Oculocerebrocutaneous Syndrome Oculodentodigital Dysplasia Oculopalatocerebral Syndrome Olfactory Neuroblastoma Oligoastrocytoma Oligodendroglioma Oligohydramnios Oliver Syndrome Olivopontocerebellar Atrophy Open-Angle Glaucoma Opiate Dependence Opioid Abuse Opitz Gbbb Syndrome, Type I Opsoclonus-Myoclonus Syndrome Optic Nerve Hypoplasia, Bilateral Optic Neuritis Optic Papillitis Optic Pathway Glioma Orbital Cellulitis Orbital Cyst Orbital Lymphangioma Ornithinemia Orofaciodigital Syndrome Orofaciodigital Syndrome Iv Orthostatic Intolerance Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteomalacia Osteomyelitis Osteomyelitis, Sterile Multifocal, with Periostitis and Pustulosis Osteonecrosis Osteopetrosis Osteopetrosis, Autosomal Recessive 3 Otitis Externa Otitis Media Ovarian Cancer Ovarian Cyst Ovarian Hyperstimulation Syndrome Pachygyria Paine Syndrome Pancreatic Adenoma Pancreatitis Pancreatitis, Hereditary Pancytopenia Panic Disorder Panuveitis Papillary Carcinoma Papilledema Papilloma Papillomatosis, Confluent and Reticulated Paraganglioma Paragonimiasis Parametritis Paraneoplastic Syndromes Paraplegia Paraquat Poisoning Parasagittal Meningioma Parathyroid Adenoma Parathyroid Carcinoma Paresthesia Parietal Foramina Parkinson Disease 15, Autosomal Recessive Early-Onset Paroxysmal Cold Hemoglobinuria Paroxysmal Nocturnal Hemoglobinuria Pasteurellosis Patent Foramen Ovale Pediatric Arterial Ischemic Stroke Pelizaeus-Merzbacher Disease Pemphigoid Gestationis Penis Agenesis Periodontal Disease Periodontitis Periostitis Peripartum Cardiomyopathy Peripheral Artery Disease Peripheral Dysostosis Peritonitis Periventricular Leukomalacia Periventricular Nodular Heterotopia Persistent Eustachian Valve Persistent Placoid Maculopathy Persistent Vegetative State Personality Disorder Pertussis Pervasive Developmental Disorder Petroclival Meningioma Phace Association Phace Syndrome Phaeochromocytoma Phaeohyphomycosis Phenylketonuria Pheochromocytoma Phimosis Pick Disease of Brain Pilocytic Astrocytoma Pineal Cyst Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities Pituitary Adenoma Pituitary Apoplexy Pituitary Carcinoma Pituitary Hormone Deficiency, Combined, 2 Pituitary Tumors Placental Abruption Placental Insufficiency Plasmacytoma Plasmodium Falciparum Malaria Plasmodium Vivax Malaria Plastic Bronchitis Pleomorphic Xanthoastrocytoma Pleuropulmonary Blastoma Plp1-Related Disorders Pmm2-Congenital Disorder of Glycosylation Pneumococcal Meningitis Pneumonia Pneumothorax, Primary Spontaneous Poems Syndrome Polyarteritis Nodosa Polycystic Kidney Disease Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy Polycystic Liver Disease Polycythemia Polycythemia Vera Polydactyly Polyhydramnios Polymicrogyria Polymyositis Polyneuropathy Polyradiculoneuropathy Pontine Hemorrhage Pontocerebellar Hypoplasia Pontocerebellar Hypoplasia, Type 2e Porencephaly Porphyria Portal Vein Thrombosis Posterior Cerebral Artery Infarction Posterior Cortical Atrophy Posterior Uveitis Postherpetic Neuralgia Post-Transplant Lymphoproliferative Disease Post-Traumatic Stress Disorder Postural Hypotension Prader-Willi Syndrome Precocious Puberty Pre-Eclampsia Premature Ejaculation Premature Menopause Premature Ovarian Failure 7 Primary Amebic Meningoencephalitis Primary Angiitis of the Central Nervous System Primary Biliary Cholangitis Primary Biliary Cirrhosis Primary Central Nervous System Lymphoma Primary Cerebellar Degeneration Primary Cutaneous Anaplastic Large Cell Lymphoma Primary Hyperoxaluria Primary Progressive Multiple Sclerosis Primrose Syndrome Prion Disease Progressive Multifocal Leukoencephalopathy Prosopagnosia Prostatitis Protein C Deficiency Protein-Losing Enteropathy Protein S Deficiency Protein Z Deficiency Proteus Syndrome Prothrombin Deficiency Pseudoachondroplasia Pseudobulbar Palsy Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ia Pseudopseudohypoparathyroidism Pseudoxanthoma Elasticum Psychotic Disorder Pulmonary Alveolar Proteinosis Pulmonary Arterio-Veinous Fistula Pulmonary Arteriovenous Fistulas Pulmonary Arteriovenous Malformation Pulmonary Blastoma Pulmonary Edema Pulmonary Embolism Pulmonary Embolism and Infarction Pulmonary Emphysema Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Fibrosis, Idiopathic Pulmonary Hypertension Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis Pulmonary Sequestration Pulmonary Tuberculosis Pulmonary Valve Stenosis Pulsating Exophthalmos Pure Autonomic Failure Pure Red-Cell Aplasia Purpura Pyelonephritis Pyle Disease Pyloric Stenosis Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency Quadriplegia Rabies Radiculopathy Raine Syndrome Rapidly Progressive Glomerulonephritis Rasmussen Encephalitis Reflex Epilepsy Reflex Sympathetic Dystrophy Refractive Error Relapsing Polychondritis Relapsing-Remitting Multiple Sclerosis Rem Sleep Behavior Disorder Renal Dysplasia Renal Hypertension Renal Nutcracker Syndrome Renal Tubular Acidosis Renovascular Hypertension Restless Legs Syndrome Reticulosarcoma Reticulum Cell Sarcoma Retinal Artery Occlusion Retinal Degeneration Retinal Disease Retinal Ischemia Retinal Vascular Disease Retinal Vein Occlusion Retinitis Retinoblastoma Retrograde Amnesia Retroperitoneal Fibrosis Retroperitoneal Liposarcoma Rett Syndrome Reversible Cerebral Vasoconstriction Syndrome Reye Syndrome Rhabdomyosarcoma Rheumatic Heart Disease Rheumatic Myocarditis Rheumatoid Arthritis Rheumatoid Vasculitis Riboflavin Deficiency Riddle Syndrome Ring Chromosome 18 Ring Chromosome 2 Ring Chromosome 22 Rocky Mountain Spotted Fever Rosai-Dorfman Disease Rubella Sagittal Sinus Thrombosis Salmonellosis Salt and Pepper Developmental Regression Syndrome Sandhoff Disease Sarcoid Meningitis Sarcoidosis 2 Sarcoma Scapuloperoneal Myopathy, X-Linked Dominant Scarlet Fever Scedosporiosis Scheie Syndrome Schistosomiasis Schizencephaly Schizoaffective Disorder Schizophrenia Schizophreniform Disorder Schizotypal Personality Disorder Scleromyxedema Scoliosis Scoliosis, Isolated 1 Scotoma Scrapie Scrub Typhus Sebastian Syndrome Seckel Syndrome Secondary Progressive Multiple Sclerosis Secondary Syphilis Seizure Disorder Semantic Dementia Semilobar Holoprosencephaly Senile Plaque Formation Sensorineural Hearing Loss Serine Deficiency Serotonin Syndrome Severe Combined Immunodeficiency Severe Hemophilia B Severe Pre-Eclampsia Shaken Baby Syndrome Shapiro Syndrome Shigellosis Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sialadenitis Sickle Cell Anemia Sickle Cell Disease Sick Sinus Syndrome Siderosis Silent Myocardial Infarction Simultanagnosia Sinusitis Situs Inversus Skeletal Dysplasias Skull Base Meningioma Sleep Apnea Sleep Disorder Sleeping Sickness Slipped Capital Femoral Epiphysis Smith-Kingsmore Syndrome Smith-Lemli-Opitz Syndrome Sneddon Syndrome Social Phobia Somatization Disorder Sotos Syndrome 1 Sparganosis Spasmodic Dysphonia Spasmodic Dystonia Spastic Ataxia, Charlevoix-Saguenay Type Spastic Cerebral Palsy Spastic Diplegia Spastic Diplegia Cerebral Palsy Spastic Hemiplegia Spasticity Spastic Paraparesis Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity Spastic Quadriplegia Speech Disorder Sphenoid Sinusitis Spina Bifida Aperta Spinal Cord Infarction Spinal Cord Injury Spinal Cord Oligodendroglioma Spinal Stenosis Spindle Cell Hemangioma Spinocerebellar Degeneration Splenic Infarction Splenic Marginal Zone Lymphoma Splenomegaly Split Hand Split Hand-Foot Malformation Split-Hand/foot Malformation 1 Spondylocarpotarsal Synostosis Syndrome Spondyloenchondrodysplasia Spondylolisthesis Spondylolysis Spondyloocular Syndrome Spondylosis Spontaneous Intracranial Hypotension Sporadic Hemiplegic Migraine Spotted Fever Squamous Cell Carcinoma St Anthony's Fire Status Epilepticus Stiff-Person Syndrome St. Louis Encephalitis Strabismus Streptococcal Meningitis Stroke, Ischemic Struma Ovarii Sturge-Weber Syndrome Stuttering Subacute Bacterial Endocarditis Subacute Delirium Subclavian Artery Aneurysm Subclavian Steal Syndrome Subcortical Arteriosclerotic Encephalopathy Subdural Empyema Subependymoma Substance Abuse Sudanophilic Cerebral Sclerosis Sudden Infant Death Syndrome Sudden Sensorineural Hearing Loss Superficial Siderosis Superior Mesenteric Artery Syndrome Supine Hypotensive Syndrome Suprabulbar Paresis, Congenital Supravalvular Aortic Stenosis Surfactant Metabolism Dysfunction, Pulmonary, 2 Surfactant Metabolism Dysfunction, Pulmonary, 3 Surfactant Metabolism Dysfunction, Pulmonary, 4 Sveinsson Chorioretinal Atrophy Swallowing Disorders Swayback Swine Influenza Sympathetic Ophthalmia Syncope Syndrome of Inappropriate Antidiuretic Hormone Synovitis Syphilis Systemic Capillary Leak Syndrome Systemic Lupus Erythematosus Systolic Heart Failure Taeniasis Takayasu Arteritis Tanycytic Ependymoma Tardive Dyskinesia Tay-Sachs Disease Telangiectasis Temporal Arteritis Temporal Lobe Epilepsy Teratocarcinoma Teratoma Teratoma with Malignant Transformation Testicular Germ Cell Cancer Tetanus Tetralogy of Fallot Thalassemia Theileriasis Thoracic Outlet Syndrome Three M Syndrome 1 Thrombocytopenia Thrombocytopenia 1 Thrombocytosis Thrombophilia Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Thumb Deformity Thunderclap Headache Thymoma Thyroid Crisis Thyroiditis Thyroid Lymphoma Tick-Borne Encephalitis Tolosa-Hunt Syndrome Tooth Disease Toxic Encephalopathy Toxocariasis Toxoplasmoză Tracheal Stenosis Tracheoesophageal Fistula Transient Cerebral Ischemia Transient Global Amnesia Transitional Cell Carcinoma Transposition of the Great Arteries Transverse Myelitis Transvestism Traumatic Brain Injury Treacher Collins Syndrome 1 Tremor Trichinosis Trichosporonosis Trichotillomania Trigeminal Neuralgia Triple X Syndrome Tropical Spastic Paraparesis Trypanosomiasis Trypanosomiasis, Human East-African Tuberculous Meningitis Tuberous Sclerosis Tuberous Sclerosis 2 Tularemia Tumefactive Multiple Sclerosis Turner Syndrome Twin-to-Twin Transfusion Syndrome Type Ii Mixed Cryoglobulinemia Typhoid Fever Tyrosinemia Tyrosinemia, Type I Ulcerative Colitis Unilateral Polymicrogyria Unilateral Retinoblastoma Univentricular Heart Uremia Uveitis Uvula, Bifid Valproate Embryopathy Van Der Woude Syndrome 1 Varicocele Vascular Dementia Vascular Disease Vasculitis Vasculopathy, Retinal, with Cerebral Leukodystrophy Venezuelan Equine Encephalitis Venous Insufficiency Ventricular Septal Defect Vertebral Artery Insufficiency Vertebral Artery Occlusion Vertebrobasilar Insufficiency Vestibular Disease Vestibular Nystagmus Viral Encephalitis Viral Meningitis Visual Agnosia Vitamin B12 Deficiency Vitreoretinal Degeneration, Snowflake Type Vogt-Koyanagi-Harada Disease Wallerian Degeneration Warburg Micro Syndrome Weber Syndrome Wegener Granulomatosis Wernicke Encephalopathy Wernicke-Korsakoff Syndrome West Syndrome Whiplash Whipple Disease Williams-Beuren Syndrome Wilms Tumor 6 Wilson Disease Wiskott-Aldrich Syndrome Wolff-Parkinson-White Syndrome Wyburn Mason's Syndrome Xanthogranulomatous Pyelonephritis Xanthoma Disseminatum Xanthomatosis X-Linked Charcot-Marie-Tooth Disease Yemenite Deaf-Blind Hypopigmentation Syndrome Zellweger Syndrome Zika Virus Infection Zygomycosis