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Cerebritis
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www.malacards.org
Clasificare anatomică Malacards
Boli neuronale
Vezi şi
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
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