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Nume Leukemia
Pagina Web
Clasificare globală Malacards Cancer diseases
Clasificari ICD10 Leukaemia, unspecified; Other specified leukaemias
Clasificare anatomică Malacards Immune diseases
Boli din aceeaşi familie Acute Leukemia; Chronic Leukemia; Subacute Leukemia

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Boli A-Z 8p11 Myeloproliferative Syndrome Aarskog-Scott Syndrome Abdominal Tuberculosis Abducens Nerve Disease Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Acalculous Cholecystitis Acanthosis Nigricans Achondroplasia Acinar Cell Carcinoma Acquired Amegakaryocytic Thrombocytopenia Acquired Angioedema Acquired Central Diabetes Insipidus Acquired Hemophilia Acquired Hemophilia a Acquired Idiopathic Sideroblastic Anemia Acquired Immunodeficiency Syndrome Acquired Pure Red Cell Aplasia Acquired Von Willebrand Syndrome Acrocallosal Syndrome Acrodermatitis Acrofacial Dysostosis, Catania Type Acrokeratosis Verruciformis Acromegaly Acth Deficiency, Isolated Acth-Secreting Pituitary Adenoma Actinic Keratosis Actinomycosis Acute Basophilic Leukemia Acute Biphenotypic Leukemia Acute Cholinergic Dysautonomia Acute Dacryocystitis Acute Disseminated Encephalomyelitis Acute Erythroid Leukemia Acute Generalized Exanthematous Pustulosis Acute Graft Versus Host Disease Acute Insulin Response Acute Interstitial Pneumonia Acute Leukemia Acute Leukemia of Ambiguous Lineage Acute Liver Failure Acute Lymphoblastic Leukemia, Childhood Acute Lymphocytic Leukemia Acute Megakaryoblastic Leukemia in Down Syndrome Acute Monoblastic Leukemia Acute Myeloblastic Leukemia with Maturation Acute Myeloblastic Leukemia Without Maturation Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Acute Myeloid Leukemia with Minimal Differentiation Acute Myeloid Leukemia with T(6;9)(p23;q34) Acute Myeloid Leukemia with T(8;16)(p11;p13) Translocation Acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation Acute Myeloid Leukemia with T(9;11)(p22;q23) Acute Myocardial Infarction Acute Non Lymphoblastic Leukemia Acute Pancreatitis Acute Panmyelosis with Myelofibrosis Acute Promyelocytic Leukemia Acute Respiratory Distress Syndrome Acute T Cell Leukemia Adams-Oliver Syndrome Adenocarcinoma Adenoiditis Adenoma Adenomatoid Tumor Adenomyosis Adenosquamous Carcinoma Adie Pupil Adult Acute Lymphocytic Leukemia Adult Acute Monocytic Leukemia Adult Respiratory Distress Syndrome Adult T-Cell Leukemia Agammaglobulinemia Aggressive Systemic Mastocytosis Aging Aicar Transformylase/imp Cyclohydrolase Deficiency Al Amyloidosis Aleukemic Leukemia Cutis Aleukemic Mast Cell Leukemia Aleukemic Monocytic Leukemia Cutis Alk-Positive Anaplastic Large Cell Lymphoma Allergic Rhinitis Alopecia Alopecia Areata Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alopecia Universalis Congenita Alpha-2-Plasmin Inhibitor Deficiency Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Thalassemia Myelodysplasia Syndrome Alpha Thalassemia-X-Linked Intellectual Disability Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alstrom Syndrome Alzheimer Disease 3 Amenorrhea Amyloidosis Amyloidosis Beta2m Analbuminemia Anal Canal Carcinoma Anaplastic Ganglioglioma Anaplastic Large Cell Lymphoma Anaplastic Oligoastrocytoma Anaplastic Oligodendroglioma Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Anemia, Congenital Dyserythropoietic, Type Ii Aneurysm Angel-Shaped Phalangoepiphyseal Dysplasia Angioedema Angioimmunoblastic T-Cell Lymphoma Angiomatosis Aniridia 1 Anorexia Nervosa 1 Anterior Scleritis Anterior Segment Dysgenesis 4 Antigen Defined by Monoclonal Antibody Aj9 Antiphospholipid Syndrome Anti-Plasmin Deficiency, Congenital Antithrombin Iii Deficiency Anuria Aortic Aneurysm Aortitis Aphasia Aplastic Anemia Apocrine Gland Secretion, Variation in Apparent Mineralocorticoid Excess Appendicitis Arbitrary Restriction Polymorphism 1 Aregenerative Anemia Argyria Arterial Thoracic Outlet Syndrome Arteries, Anomalies of Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 7 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Arthropathy Aryl Hydrocarbon Hydroxylase Inducibility Asbestos Intoxication Asbestosis Aseptic Meningitis Asparagine Synthetase Deficiency Aspergillosis Aspergillus Niger Infection Asthma Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Ataxia-Pancytopenia Syndrome Ataxia-Telangiectasia Atrichia with Papular Lesions Attention Deficit-Hyperactivity Disorder Atypical Chronic Myeloid Leukemia Atypical Teratoid Rhabdoid Tumor Australia Antigen Autoimmune Disease Autoimmune Hepatitis Autoimmune Lymphoproliferative Syndrome, Type V Autoimmune Pancreatitis Autoimmune Polyendocrine Syndrome Autoinflammation with Infantile Enterocolitis Autonomic Neuropathy Axenfeld-Rieger Syndrome Axonal Neuropathy Bacillary Angiomatosis Back Pain Balanoposthitis B- and T-Cell Mixed Leukemia Baraitser-Winter Cerebrofrontofacial Syndrome Baraitser-Winter Syndrome 1 Barrett Esophagus Basal Cell Carcinoma B-Cell Adult Acute Lymphocytic Leukemia B-Cell Expansion with Nfkb and T-Cell Anergy B-Cell Growth Factor B Cell Linker Protein Deficiency B-Cell Lymphomas B Cell Prolymphocytic Leukemia Beckwith-Wiedemann Syndrome Bernard-Soulier Syndrome Beta-Thalassemia Bilateral Breast Cancer Biotinidase Deficiency Bjornstad Syndrome Bk-Virus Nephropathy Bladder Cancer Blastic Plasmacytoid Dendritic Cell Blastomycosis Bleeding Disorder, Platelet-Type, 11 Blepharochalasis Blepharoconjunctivitis Blood Group--Ahonen Blood Group, Dombrock System Blood Group Incompatibility Blood Group, I System Blood Platelet Disease Bloom Syndrome Blue Rubber Bleb Nevus Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Boerhaave Syndrome Bone Fracture Bone Marrow Cancer Bone Marrow Necrosis Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Borna Disease Bowenoid Papulosis Brachial Plexus Neuropathy Brain Cancer Brain Edema Brain Sarcoma Brain Small Vessel Disease with or Without Ocular Anomalies Breast Adenocarcinoma Breast Cancer Broken Heart Syndrome Bronchiolitis Bronchiolitis Obliterans Bronchopneumonia Brooke-Spiegler Syndrome Brucellosis Brugada Syndrome Budd-Chiari Syndrome Bullous Pemphigoid Burkitt Lymphoma Burns Buruli Ulcer C3 Glomerulopathy Calcinosis Calciphylaxis Candida Glabrata Candidiasis Capillary Leak Syndrome Cardiac Arrest Cardiac Tamponade Cardiomyopathy, Familial Hypertrophic, 1 Carotidynia Castleman Disease Cataract Cataract 2, Multiple Types Cataract 5, Multiple Types Cat-Scratch Disease Cauda Equina Syndrome Cavernous Malformation Cavernous Sinus Thrombosis Cd4/cd8 T-Cell Ratio Cellulitis Central Nervous System Disease Central Nervous System Leukemia Central Nervous System Lymphoma Central Nervous System Origin Vertigo Central Nervous System Vasculitis Central Neurocytoma Central Pontine Myelinolysis Central Retinal Vein Occlusion Central Serous Chorioretinopathy Central Sleep Apnea Cerebellar Angioblastoma Cerebellar Astrocytoma Cerebellar Degeneration-Related Autoantigen 3 Cerebral Atrophy Cerebral Degeneration Cerebral Hemorrhage Cerebral Lymphoma Cerebral Meningioma Cerebral Sinovenous Thrombosis Cerebritis Cervical Cancer Cervicitis Charcot-Marie-Tooth Disease Chediak-Higashi Syndrome Cheilitis Chickenpox Childhood Apraxia of Speech Childhood Leukemia Cholangiocarcinoma Cholecystitis Cholera Chops Syndrome Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choriocarcinoma Choroiditis Chromosomal Triplication Chromosome 11q Duplication Chromosome 12p Deletion Chromosome 13q14 Deletion Syndrome Chromosome 16p13.3 Deletion Syndrome, Proximal Chromosome 16 Trisomy Chromosome 17p Deletion Chromosome 20q Deletion Chromosome 3q29 Deletion Syndrome Chromosome 5q Deletion Syndrome Chromosome 6q Deletion Chromosome Xq Duplication Chronic Actinic Dermatitis Chronic Active Epstein-Barr Virus Infection Chronic Enteropathy Associated with Slco2a1 Gene Chronic Eosinophilic Leukemia Chronic Fatigue Syndrome Chronic Graft Versus Host Disease Chronic Granulomatous Disease Chronic Inflammatory Demyelinating Polyneuropathy Chronic Leukemia Chronic Meningitis Chronic Monocytic Leukemia Chronic Myelomonocytic Leukemia Chronic Neutrophilic Leukemia Chronic Recurrent Multifocal Osteomyelitis Chronic Rhinitis Chylomicron Retention Disease Classic Hairy Cell Leukemia Classic Phenylketonuria Cleft Lip Cleft Lip/palate with Abnormal Thumbs and Microcephaly Cleidocranial Dysplasia Cll/sll Clostridium Difficile Colitis Clostridium Septicum Infection Coccidiosis Cohen-Gibson Syndrome Cohen Syndrome Cold Agglutinin Disease Colitis Collagen Disease Colon Adenocarcinoma Colonic Pseudo-Obstruction Colorblindness, Partial, Protan Series Colorectal Cancer Colorectal Cancer 3 Common Variable Immunodeficiency Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Composite Lymphoma Congenital Anomalies of Kidney and Urinary Tract 2 Congenital Bile Acid Synthesis Defect Congenital Cytomegalovirus Congenital Disorder of Glycosylation, Type Iic Congenital Dyserythropoietic Anemia Congenital Fibrosarcoma Congenital Human Immunodeficiency Virus Congenital Hypoplastic Anemia Congenital Syphilis Congestive Heart Failure Conidiobolomycosis Conjunctivitis Connective Tissue Disease Conotruncal Heart Malformations Constipation Constrictive Pericarditis Conversion Disorder Core Binding Factor Acute Myeloid Leukemia Corneal Dystrophy, Avellino Type Cornelia De Lange Syndrome Cortical Blindness Cortisone Reductase Deficiency 1 Coumarin Resistance Cranial Nerve Palsy Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Craniopharyngioma Crescentic Glomerulonephritis Critical Illness Polyneuropathy Crohn's Colitis Crohn's Disease Crouzon Syndrome Crouzon Syndrome with Acanthosis Nigricans Cryoglobulinemia Cryptococcal Meningitis Cryptococcosis Cryptogenic Organizing Pneumonia Cryptosporidiosis Cutaneous Mastocytosis Cutaneous T Cell Lymphoma Cutis Verticis Gyrata Cystadenocarcinoma Cystic Fibrosis Cystinuria Cystitis Cytochrome P450 2d6 Variant Cytogenetically Normal Acute Myeloid Leukemia Cytomegalic Inclusion Disease Cytomegalovirus Infection Cytomegalovirus Retinitis Dacryoadenitis Dacryocystitis Darier-White Disease Dedifferentiated Liposarcoma Demodicidosis Demyelinating Disease Demyelinating Polyneuropathy Dendritic Cell Tumor Dengue Virus Dermatitis Dermatitis Herpetiformis Dermatomyositis Dermatophytosis Desmoplastic Small Round Cell Tumor Dextrocardia Diabetes Insipidus Diabetes Mellitus Diamond-Blackfan Anemia Diarrhea Diarrhea 2, with Microvillus Atrophy Diffuse Alveolar Hemorrhage Diffuse Large B-Cell Lymphoma Diphtheria Discitis Disseminated Eosinophilic Collagen Disease Disseminated Intravascular Coagulation Down Syndrome Drug-Induced Autoimmune Hemolytic Anemia Duane Retraction Syndrome 1 Duodenal Atresia Duodenitis Dwarfism Dyschromatosis Symmetrica Hereditaria Dysentery Dysfibrinogenemia Dyskeratosis Congenita Eating Disorder Ecthyma Ectodermal Dysplasia Ectopic Pregnancy Ectopic Thymus Ehrlichiosis Elliptocytosis 1 Embryonal Carcinoma Empty Sella Syndrome Encephalitis Encephalitozoonosis Encephalopathy Endocardial Fibroelastosis Endocarditis Endocrine Gland Cancer Endometrial Adenocarcinoma Endometriosis Endomyocardial Fibrosis Endophthalmitis Endotheliitis End Stage Renal Failure Enterocolitis Enteropathica Enterovesical Fistula Eosinophilia-Myalgia Syndrome Eosinophilic Fasciitis Eosinophilic Meningitis Epidermodysplasia Verruciformis Epidermolysis Bullosa Pruriginosa Epididymo-Orchitis Epidural Abscess Epiglottitis Epilepsy Epilepsy, Pyridoxine-Dependent Epithelial Recurrent Erosion Dystrophy Epstein-Barr Virus-Positive Diffuse Large B-Cell Lymphoma of the Elderly Erdheim-Chester Disease Erysipelas Erythema Elevatum Diutinum Erythema Infectiosum Erythema Multiforme Erythroleukemia, Familial Erythromelalgia Esophageal Cancer Esophageal Candidiasis Esotropia Essential Thrombocythemia Estrogen Resistance Ewing's Family of Tumors Ewing Sarcoma Exanthem Exfoliative Dermatitis Exophthalmos Extracutaneous Mastocytoma Extramedullary Plasmacytoma Extrapontine Myelinolysis Facial Paralysis Factor V Deficiency Factor Vii Deficiency Factor X Deficiency Factor Xiii Deficiency Fallopian Tube Endometrioid Adenocarcinoma Familial Adenomatous Polyposis Familial Mediterranean Fever Fanconi Anemia, Complementation Group a Fanconi Anemia, Complementation Group D2 Fanconi Anemia, Complementation Group E Fanconi-Bickel Syndrome Fanconi Syndrome Fasciitis Fasting Hypoglycemia Felty Syndrome Fibrosarcoma Fibrous Dysplasia Fibrous Histiocytoma Fibular Hypoplasia and Complex Brachydactyly Filariasis Focal Segmental Glomerulosclerosis Follicular Dendritic Cell Sarcoma Follicular Lymphoma Follicular Mucinosis Folliculitis Fontaine Progeroid Syndrome Foot Drop Fragile Site 10q25 Friedreich Ataxia 1 Fructose Utilization Fundus Albipunctatus Fusariosis Galactorrhea Gallbladder Adenocarcinoma Gallbladder Cancer Gamma Heavy Chain Disease Ganglioglioma Ganglioneuroblastoma Ganglioneuroma Gas Gangrene Gastric Adenocarcinoma Gastric Antral Vascular Ectasia Gastric Cancer Gastric Lymphoma Gastric Ulcer Gastritis Gastroenteritis Gastrointestinal Stromal Tumor Gaucher Disease, Type Iii Generalized Eruptive Histiocytosis Genital Herpes Genitopatellar Syndrome Germ Cells Tumors Gerstmann Syndrome Giardioză Gilbert Syndrome Gilles De La Tourette Syndrome Gingival Hypertrophy Gingivitis Gitelman Syndrome Glanzmann Thrombasthenia Glaucoma-Related Pigment Dispersion Syndrome Glioblastoma Glioblastoma Multiforme Glioma Glomerulonephritis Glossitis Glucocorticoid Resistance, Generalized Glucose/galactose Malabsorption Glucose Transporter Type 1 Deficiency Syndrome Glycogen Storage Disease Glycogen Storage Disease V Goblet Cell Carcinoid Gonadal Dysgenesis Good Syndrome Graft-Versus-Host Disease Granulocytopenia Granuloma Annulare Granulomatous Amebic Encephalitis Granulomatous Angiitis Granulomatous Dermatitis Granulomatous Gastritis Granulomatous Hepatitis Granulomatous Rosacea Graves' Disease Griscelli Syndrome Grover's Disease Growing Teratoma Syndrome Growth Control, Y-Chromosome Influenced Growth Hormone Deficiency Guillain-Barre Syndrome Guttate Psoriasis Gynecomastia Haemophilus Influenzae Hairy Cell Leukemia Hajdu-Cheney Syndrome Hansen's Disease Hantavirus Pulmonary Syndrome Headache Headache Associated with Sexual Activity Heavy Chain Disease Helicobacter Pylori Infection Helix Syndrome Hellp Syndrome Hemangioma Hemarthrosis Hematologic Cancer Hematopoietic Stem Cell Transplantation Hemochromatosis, Neonatal Hemochromatosis, Type 1 Hemochromatosis, Type 2a Hemoglobin H Disease Hemoglobinuria Hemolytic Anemia Hemolytic Anemia, Cd59-Mediated, with or Without Immune-Mediated Polyneuropathy Hemolytic-Uremic Syndrome Hemopericardium Hemophagocytic Lymphohistiocytosis Hemophagocytic Lymphohistiocytosis, Familial, 2 Hemophilia Hemophilia a Hemophilic Arthropathy Hemorrhagic Cystitis Hemosiderosis Hepatic Adenomas, Familial Hepatic Veno-Occlusive Disease Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis E Hepatoblastoma Hepatocellular Carcinoma Hepatorenal Syndrome Hepatosplenic T-Cell Lymphoma Hereditary Hemorrhagic Telangiectasia Hereditary Multiple Exostoses Hereditary Spherocytosis Hereditary Wilms' Tumor Herpes Simplex Herpes Zoster Herpetic Whitlow Heterotaxy, Visceral, 2, Autosomal Hhv-6 Encephalitis Hidradenitis Histiocytic Sarcoma Histiocytoma Histiocytosis Histiocytosis-Lymphadenopathy Plus Syndrome Histoplasmosis Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis Human Herpesvirus 8 Human Immunodeficiency Virus Type 1 Human Monocytic Ehrlichiosis Human T-Cell Leukemia Virus Type 1 Human T-Cell Leukemia Virus Type 2 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius Hydrolethalus Syndrome 1 Hydronephrosis Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperaldosteronism, Familial, Type I Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant Hypereosinophilic Syndrome Hyperglycemia Hyper Ige Syndrome Hyperostosis Hyperoxaluria, Primary, Type I Hyperparathyroidism Hyperphenylalaninemia Hyperphenylalaninemia, Bh4-Deficient, C Hyperphosphatemia Hyperreflexia Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypertrichosis Hypertrophy of Breast Hyperuricemia Hypoaldosteronism Hypoglycemia Hypokalemia Hypoparathyroidism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatasia Hypophosphatemia Hypopituitarism Hypopyon Hyporeninemic Hypoaldosteronism Hypotonia-Cystinuria Syndrome Hypotrichosis 1 Hypoxia Ichthyosis Ichthyosis Prematurity Syndrome Ichthyosis Vulgaris Idiopathic Neutropenia Igg4-Related Hepatopathy Immune-Complex Glomerulonephritis Immune Suppression Immunodeficiency 21 Immunodeficiency 43 Immunodeficiency with Hyper-Igm, Type 2 Immunoglobulin Alpha Deficiency Immunoglobulin E Concentration, Serum Immunotactoid Glomerulopathy Inclusion Body Myositis Incontinentia Pigmenti Indeterminate Cell Histiocytosis Indolent B Cell Lymphoma Infant Gynecomastia Infective Dermatitis Associated with Htlv-1 Infective Endocarditis Infertility Inflammatory Bowel Disease 1 Influenza Inherited Bone Marrow Failure Syndromes Insulin-Like Growth Factor I Intellectual Disability-Developmental Delay-Contractures Syndrome Interdigitating Dendritic Cell Sarcoma Interleukin-7 Receptor Alpha Deficiency Intermediate Uveitis Interstitial Nephritis Intervertebral Disc Disease Intestinal Perforation Intestinal Pseudo-Obstruction Intracranial Hypertension Intraocular Melanoma Intravascular Large B-Cell Lymphoma Intraventricular Meningioma Intussusception Invasive Aspergillosis Iridocyclitis Ischemia Isolated Delta-Storage Pool Disease Jackson-Weiss Syndrome Jacobsen Syndrome Janus Kinase-3 Deficiency Juvenile Myelomonocytic Leukemia Juvenile Pilocytic Astrocytoma Juvenile Polyposis/hereditary Hemorrhagic Telangiectasia Syndrome Juvenile Rheumatoid Arthritis Juvenile Xanthogranuloma Kabuki Syndrome 1 Kallmann Syndrome Kaposiform Hemangioendothelioma Kaposi Sarcoma Keloids Keratoacanthoma Keratomalacia Keratosis Kidney Cancer Kidney Cortex Necrosis Kikuchi Disease Kindler Syndrome Kniest Dysplasia Knobloch Syndrome Lacrimal Gland Carcinoma Lactic Acidosis Lambert-Eaton Myasthenic Syndrome Lambert Syndrome Langerhans Cell Histiocytosis Langerhans Cell Sarcoma Large Granular Lymphocyte Leukemia Laryngeal Adductor Paralysis Laryngeal Cleft Laryngitis Lateral Sclerosis Leber Hereditary Optic Neuropathy Legionellosis Legionnaire Disease Legionnaires' Disease Leiomyoma Leiomyosarcoma Leishmaniasis Leopard Syndrome Lepromatous Leprosy Letterer-Siwe Disease Leukemia, Acute Lymphoblastic Leukemia, Acute Lymphoblastic 3 Leukemia, Acute Monocytic Leukemia, Acute Myeloid Leukemia, B-Cell, Chronic Leukemia, Chronic Lymphocytic Leukemia, Chronic Lymphocytic 2 Leukemia, Chronic Myeloid Leukemia, T-Cell, Chronic Leukodystrophy, Hypomyelinating, 5 Leukoplakia Leukostasis Leukotriene C4 Synthase Deficiency Lichen Nitidus Lichen Sclerosus Lichen Sclerosus Et Atrophicus Li-Fraumeni Syndrome Li-Fraumeni Syndrome 2 Limb-Girdle Muscular Dystrophy Limbic Encephalitis Limb Ischemia Linitis Plastica Lipodystrophy Lipodystrophy, Partial, Acquired Lipoid Nephrosis Liposarcoma Lissencephaly 1 Listeriosis Liver Disease Liver Inflammatory Pseudotumor Loeffler Endocarditis Logopenic Progressive Aphasia Long Qt Syndrome Lung Abscess Lung Cancer Lupus Erythematosus Luscan-Lumish Syndrome Lutheran Suppressor, X-Linked Lymphadenitis Lymphangitis Lymphedema Lymphedema, Hereditary, Ia Lymph Node Tuberculosis Lymphoblastic Leukemia Lymphoblastic Leukemia, Acute, with Lymphomatous Features Lymphoblastic Lymphoma Lymphocytic Choriomeningitis Lymphocytic Vasculitis Lymphoid Interstitial Pneumonia Lymphoid Leukemia Lymphoma Lymphoma, Hodgkin, Classic Lymphomatoid Granulomatosis Lymphomatoid Papulosis Lymphopenia Lymphoplasmacytic Lymphoma Lymphosarcoma Macrocytic Anemia Macroglobulinemia Macs Syndrome Malakoplakia Malaria Malignant Germ Cell Tumor Malignant Histiocytosis Malignant Hyperthermia Malignant Spiradenoma Malignant Teratoma Malignant Triton Tumor Mannose-Binding Lectin Deficiency Mantle Cell Lymphoma Marantic Endocarditis Marden-Walker Syndrome Marginal Zone B-Cell Lymphoma Mast Cell Disease Mast-Cell Leukemia Mast Cell Neoplasm Mast-Cell Sarcoma Mature B-Cell Neoplasm Mckusick-Kaufman Syndrome Measles Meckel Syndrome, Type 1 Meconium Ileus Mediastinitis Medullary Sponge Kidney Medulloblastoma Megacolon Megakaryocytic Leukemia Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 Megaloblastic Anemia Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency Melanoma Melanoma-Astrocytoma Syndrome Melanoma, Cutaneous Malignant 8 Melioidosis Melkersson-Rosenthal Syndrome Membranoproliferative Glomerulonephritis Meningioma, Familial Meningitis Meningococcemia Meningoencephalitis Menkes Disease Meralgia Paresthetica Merkel Cell Carcinoma Methemoglobinemia Microcephalic Osteodysplastic Primordial Dwarfism, Type I Microcephaly 1, Primary, Autosomal Recessive Microcephaly, Epilepsy, and Diabetes Syndrome Microphthalmia Microsporidiosis Migraine with Aura Miliaria Miliary Tuberculosis Miller-Dieker Lissencephaly Syndrome Miller Fisher Syndrome Mirage Syndrome Mismatch Repair Cancer Syndrome Mite Infestation Mitochondrial Import-Stimulating Factor Mixed Connective Tissue Disease Mixed Germ Cell Tumor Mixed-Type Autoimmune Hemolytic Anemia Miyoshi Muscular Dystrophy 1 Mn1 Molluscum Contagiosum Monocytic Leukemia Mononeuritis Multiplex Monosomy 21 Monosomy 7 of Bone Marrow Mood Disorder Mosaic Trisomy 8 Mosaic Trisomy 9 Mowat-Wilson Syndrome Moyamoya Disease 1 Mucocele of Salivary Gland Mucoepidermoid Carcinoma Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Vii Mucositis Muenke Syndrome Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Multiple Acyl-Coa Dehydrogenase Deficiency Multiple Cranial Nerve Palsy Multiple Enchondromatosis, Maffucci Type Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Mumps Mungan Syndrome Muscular Dystrophy Muscular Dystrophy, Limb-Girdle, Type 1a Musical Perfect Pitch Myasthenia Gravis Myasthenic Syndrome, Congenital, 4c, Associated with Acetylcholine Receptor Deficiency Mycetoma Mycobacterium Abscessus Mycobacterium Chelonae Mycobacterium Fortuitum Mycobacterium Kansasii Mycobacterium Malmoense Mycobacterium Marinum Mycosis Fungoides Myelitis Myelodysplastic Myeloproliferative Cancer Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloid Sarcoma Myeloma, Multiple Myeloperoxidase Deficiency Myelophthisic Anemia Myeloproliferative Neoplasm Myeloproliferative Syndrome, Transient Myhre Syndrome Myocardial Infarction Myocarditis Myoclonic-Astastic Epilepsy Myoclonic Epilepsy of Lafora Myoclonus, Familial Cortical Myopathy Myopathy, Tubular Aggregate, 1 Myopathy with Lactic Acidosis, Hereditary Myositis Myositis Ossificans Myxedema Myxoid Liposarcoma Nasopharyngeal Carcinoma Nasopharyngitis Natural Killer Cell Leukemia Necrobiotic Xanthogranuloma Necrotizing Fasciitis Necrotizing Ulcerative Gingivitis Neonatal Leukemia Nephrocalcinosis Nephrosclerosis Nephrotic Syndrome Nervous System Cancer Nervous System Disease Neuraminidase Deficiency Neurilemmoma Neuritis Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neuroendocrine Tumor Neurofibromatosis-Noonan Syndrome Neurofibromatosis, Type I Neurofibromatosis, Type Iv, of Riccardi Neuronitis Neuropathy Neuroretinitis Neutropenia Neutropenia, Nonimmune Chronic Idiopathic, of Adults Neutropenia, Severe Congenital, 3, Autosomal Recessive Neutrophil Actin Dysfunction Neutrophilia, Hereditary Neutrophilic Dermatosis, Acute Febrile Neutrophil Migration Newcastle Disease Nicolaides-Baraitser Syndrome Niemann-Pick Disease Niemann-Pick Disease, Type C1 Nijmegen Breakage Syndrome Nocardiosis Nodular Regenerative Hyperplasia Noma Non-Involuting Congenital Hemangioma Nonseminomatous Germ Cell Tumor Norwegian Scabies Null-Cell Leukemia Obstructive Jaundice Occipital Horn Syndrome Ocular Hypertension Ocular Melanoma Oculotrichodysplasia Okt4 Epitope Deficiency Olfactory Neuroblastoma Oligoastrocytoma Oligodendroglioma Oliver Syndrome Optic Neuritis Oral Cancer Oral Candidiasis Oral Hairy Leukoplakia Oral Squamous Cell Carcinoma Orbital Cancer Orchitis Osteomyelitis Osteomyelitis, Sterile Multifocal, with Periostitis and Pustulosis Osteonecrosis Osteopetrosis Otitis Externa Otospondylomegaepiphyseal Dysplasia, Autosomal Recessive Ovarian Cancer Ovarian Serous Cystadenocarcinoma Overhydrated Hereditary Stomatocytosis Paine Syndrome Pancreatic Cancer Pancreatitis Pancreatitis, Hereditary Pancytopenia Panniculitis Panuveitis Papillary Carcinoma Papilledema Papilloma Papillon-Lefevre Syndrome Papular Mucinosis Parainfluenza Virus Type 3 Paralytic Ileus Paralytic Poliomyelitis Paraneoplastic Pemphigus Paraneoplastic Syndromes Paraplegia Parkinson Disease 2, Autosomal Recessive Juvenile Parkinsonism with Spasticity, X-Linked Paronychia Parotitis Paroxysmal Nocturnal Hemoglobinuria Pdgfra-Associated Chronic Eosinophilic Leukemia Pdgfrb-Associated Chronic Eosinophilic Leukemia Pediatric Lymphoma Pelger-Huet Anomaly Pemphigus Pemphigus Foliaceus Pericardial Effusion Pericardial Tuberculosis Pericarditis Pericoronitis Periodontal Ehlers-Danlos Syndrome Periostitis Peripartum Cardiomyopathy Peripheral T-Cell Lymphoma Peritonitis Perivascular Epithelioid Cell Tumor Pernicious Anemia Persistent Polyclonal B-Cell Lymphocytosis Pertussis Pfeiffer Syndrome Phaeohyphomycosis Pharyngitis Phelan-Mcdermid Syndrome Phenylketonuria Pheochromocytoma Philadelphia-Negative Chronic Myeloid Leukemia Pick Disease of Brain Pilocytic Astrocytoma Pineal Gland Cancer Pitt-Hopkins Syndrome Pituitary Adenoma Pituitary Apoplexy Pituitary Hormone Deficiency, Combined, 2 Pituitary Stalk Interruption Syndrome Pituitary Tumors Pityriasis Lichenoides Pityriasis Rotunda Pityriasis Rubra Pilaris Placental Abruption Plasmablastic Lymphoma Plasma Cell Leukemia Plasma Cell Neoplasm Plasmacytic Leukemia Plasmacytoma Platelet Disorder, Familial, with Associated Myeloid Malignancy Pleomorphic Adenoma Pleurisy Pleuropneumonia Plexopathy Pneumatosis Cystoides Intestinalis Pneumonia Pneumothorax Poems Syndrome Poland Syndrome Poliomyelitis Polyclonal Hypergammaglobulinemia Polycythemia Polycythemia Vera Polykaryocytosis Inducer Polymicrogyria, Bilateral Perisylvian, X-Linked Polymorphic Reticulosis Polymyositis Polyneuropathy Polyradiculoneuropathy Polyradiculopathy Polysubstance Abuse Pompholyx Porokeratosis Porphyria Porphyria Cutanea Tarda Porphyria Variegata Portal Hypertension Portal Vein Thrombosis Posterior Column Ataxia Posterior Column Ataxia with Retinitis Pigmentosa Posterior Scleritis Potocki-Lupski Syndrome Precocious Puberty Precursor T-Cell Acute Lymphoblastic Leukemia Precursor T-Lymphoblastic Lymphoma/leukemia Prekallikrein Deficiency Priapism Prieto X-Linked Mental Retardation Syndrome Primary Biliary Cirrhosis Primary Central Nervous System Lymphoma Primary Cutaneous Anaplastic Large Cell Lymphoma Primary Cutaneous Cd4+ Small/medium-Sized Pleomorphic T-Cell Lymphoma Primary Cutaneous Follicle Center Lymphoma Primary Effusion Lymphoma Primary Hyperparathyroidism Primary Lateral Sclerosis, Adult, 1 Primary Polycythemia Progressive Multifocal Leukoencephalopathy Proliferative Glomerulonephritis Prolymphocytic Leukemia Prostate Cancer Prostatitis Protein C Deficiency Protein-Losing Enteropathy Protein S Deficiency Protein Z Deficiency Prothrombin Deficiency Pseudobulbar Palsy Pseudohermaphroditism Pseudo Pelger-Huet Anomaly Psoriasis Psoriasis 13 Psoriasis 2 Psoriasis 7 Ptosis Pulmonary Alveolar Proteinosis Pulmonary Aspergilloma Pulmonary Edema Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hemosiderosis Pulmonary Hypertension Pulmonary Neuroendocrine Tumor Pulmonary Sarcoidosis Pulmonary Sequestration Pure Red-Cell Aplasia Purpura Purpura Fulminans Pustulosis Palmaris Et Plantaris Pyelonephritis Pyoderma Pyoderma Gangrenosum Pyogenic Granuloma Pyomyositis Pyridoxine Deficiency Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia Pyruvate Kinase Deficiency of Red Cells Q Fever Quadriplegia Rabies Radiculopathy Ramer Ladda Syndrome Rapadilino Syndrome Rapidly Progressive Glomerulonephritis Rapp-Hodgkin Syndrome Reactive Arthritis Recurrent Acute Pancreatitis Refractory Anemia Refractory Anemia with Excess Blasts Refractory Anemia with Excess Blasts in Transformation Refractory Celiac Disease Refractory Hairy Cell Leukemia Refsum Disease, Classic Relapsing Polychondritis Renal Cell Carcinoma, Nonpapillary Renal Tubular Acidosis Respiratory Syncytial Virus Infectious Disease Restrictive Cardiomyopathy Reticulosarcoma Reticulum Cell Sarcoma Retinal Detachment Retinal Ischemia Retinal Vasculitis Retinal Vein Occlusion Retinitis Retinitis Pigmentosa Retinoblastoma Retroperitoneal Fibrosis Rett Syndrome Reversible Cerebral Vasoconstriction Syndrome Rhabdomyosarcoma Rheumatic Fever Rheumatic Fever-Related Antigen Rheumatoid Arthritis Rhinitis Richter's Syndrome Riddle Syndrome Ring Chromosome 1 Ring Chromosome 10 Ring Chromosome 11 Ring Chromosome 16 Ring Chromosome 18 Ring Chromosome 2 Ring Chromosome 21 Ring Chromosome 5 Ring Chromosome 6 Ring Chromosome 7 Ring Chromosome 8 Roberts Syndrome Rosacea Rosai-Dorfman Disease Rubella Sagittal Sinus Thrombosis Sarcoidosis 2 Sarcoma Satb2-Associated Syndrome Scabies Scedosporiosis Schizophrenia Scleritis Scleromalacia Perforans Scleromyxedema Sclerosing Cholangitis, Neonatal Scott Syndrome Sea-Blue Histiocyte Disease Sebaceous Adenoma Sebastian Syndrome Secondary Pulmonary Alveolar Proteinosis Seminoma Septic Arthritis Serous Cystadenocarcinoma Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Severe Combined Immunodeficiency Severe Combined Immunodeficiency, X-Linked Severe Congenital Neutropenia Sezary's Disease Short Bowel Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Shwachman-Diamond Syndrome Sialadenitis Sickle Cell Anemia Sickle Cell Disease Sideroblastic Anemia Siderosis Sinusitis Situs Inversus Sjogren-Larsson Syndrome Skin Benign Neoplasm Skin Disease Skin Hemangioma Sleep Apnea Sm-Ahnmd Small Cell Carcinoma Small Intestinal Sarcoma Small Non-Cleaved Cell Lymphoma Smith-Kingsmore Syndrome Smoldering Myeloma Smooth Muscle Tumor Soft Tissue Sarcoma Sotos Syndrome 1 Spastic Ataxia, Charlevoix-Saguenay Type Spasticity Spastic Paraparesis Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity Spherocytosis, Type 1 Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinal Cord Injury Spindle Cell Carcinoma Spiradenoma Splenic Abscess Splenic Diffuse Red Pulp Small B-Cell Lymphoma Splenic Infarction Splenic Marginal Zone Lymphoma Splenic Sequestration Splenic Tuberculosis Splenomegaly Spondylitis Spondyloarthropathy 1 Spondylocarpotarsal Synostosis Syndrome Spondyloocular Syndrome Sporotrichosis Squamous Cell Carcinoma Squamous Cell Carcinoma of the Larynx Status Asthmaticus Steatocystoma Multiplex Stenotrophomonas Maltophilia Infection Steroid-Induced Glaucoma Stomatitis Storage Pool Platelet Disease Streptococcal Meningitis Strongyloidiasis Sturge-Weber Syndrome Stuve-Wiedemann Syndrome Subacute Bacterial Endocarditis Subacute Leukemia Subacute Monocytic Leukemia Subleukemic Leukemia Suppression of Tumorigenicity 12 Suppurative Thyroiditis Sveinsson Chorioretinal Atrophy Syncope Syndrome of Inappropriate Antidiuretic Hormone Synovitis Syphilis Syringoma Systemic Capillary Leak Syndrome Systemic Lupus Erythematosus Systemic Mastocytosis Systemic Onset Juvenile Idiopathic Arthritis Takayasu Arteritis Tarsal-Carpal Coalition Syndrome Tarsal Tunnel Syndrome Tatton-Brown-Rahman Syndrome T Cell Deficiency T-Cell Large Granular Lymphocyte Leukemia T-Cell Leukemia T-Cell Lymphoma 1a T-Cell Prolymphocytic Leukemia Temporal Arteritis Temporal Lobe Epilepsy Teratocarcinoma Teratoma Testicular Cancer Testicular Disease Testicular Germ Cell Tumor Testicular Germ Cell Tumor 1 Testicular Leukemia Testicular Seminoma Tetanus Tetraploidy Tetrasomy 21 Tetrasomy 5p Thalassemia Therapy Related Acute Myeloid Leukemia and Myelodysplastic Syndrome Thiopurines, Poor Metabolism of, 1 Thoracoabdominal Syndrome Three M Syndrome 1 Thrombasthenia Thrombocytopenia Thrombocytopenia 1 Thrombocytosis Thrombophilia Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Thymic Hyperplasia Thymoma Thyroid Cancer Thyroid Cancer, Nonmedullary, 1 Thyroiditis Thyroid Lymphoma Timothy Syndrome Tl Antigen Tongue Cancer Tonsillitis Tooth Disease Toxic Encephalopathy Toxic Megacolon Toxoplasmoză Tracheal Stenosis Tracheoesophageal Fistula Treacher Collins Syndrome 1 Trichosporonosis Trigeminal Neuralgia Triploidy Trisomy 1q Trisomy 22 Trisomy 2 Mosaicism Tropical Spastic Paraparesis Tuberculous Meningitis Tuberous Sclerosis Tuberous Sclerosis 1 Tuberous Sclerosis 2 Turner Syndrome Ulcerative Colitis Ulnar Hypoplasia Unilateral Retinoblastoma Ureteral Obstruction Urticaria Urticaria Pigmentosa Uruguay Faciocardiomusculoskeletal Syndrome Uveitis Valproate Embryopathy Van Der Woude Syndrome 1 Vasculitis Velocardiofacial Syndrome Viral Exanthem Viral Hepatitis Viral Meningitis Virus Associated Hemophagocytic Syndrome Virus-Associated Trichodysplasia Spinulosa Visceral Leishmaniasis Vitamin B12 Deficiency Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Vogt-Koyanagi-Harada Disease Waldenstrom Macroglobulinemia Warthin Tumor Weaver Syndrome Weber Syndrome Wells Syndrome Werner Syndrome Wernicke Encephalopathy West Nile Virus Whim Syndrome Williams-Beuren Syndrome Wilms Tumor 1 Wilms Tumor 6 Wilson Disease Wilson-Turner X-Linked Mental Retardation Syndrome Wiskott-Aldrich Syndrome Witkop Syndrome Xanthogranulomatous Pyelonephritis X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome Zinc-Responsive Necrolytic Acral Erythema Zygomycosis