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Nume Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity
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Clasificare globală Malacards Genetic diseases; Rare diseases
Clasificari ICD10 Other combined immunodeficiencies
Clasificare anatomică Malacards Blood diseases; Immune diseases

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Boli A-Z 49,xxxxy Syndrome Aarskog-Scott Syndrome Abdominal Tuberculosis Acanthosis Nigricans Aceruloplasminemia Achalasia Achalasia, Familial Esophageal Acid Phosphatase Deficiency Acquired Angioedema Acquired Generalized Lipodystrophy Acquired Hemophilia Acquired Hemophilia a Acquired Immunodeficiency Syndrome Acquired Von Willebrand Syndrome Acrodermatitis Acth Deficiency, Isolated Acute Adrenal Insufficiency Acute Diarrhea Acute Disseminated Encephalomyelitis Acute Hemorrhagic Leukoencephalitis Acute Insulin Response Acute Interstitial Pneumonia Acute Leukemia Acute Liver Failure Acute Lymphocytic Leukemia Acute Myocardial Infarction Acute Myocarditis Acute Necrotizing Encephalitis Acute Pancreatitis Acute Promyelocytic Leukemia Acute Respiratory Distress Syndrome Acute Transverse Myelitis Acute Zonal Occult Outer Retinopathy Adenocarcinoma Adenofibroma Adenohypophysitis Adenoma Adenosine Deaminase Deficiency Adiponectin, Serum Level of, Quantitative Trait Locus 1 Adrenal Cortical Hypofunction Adult Dermatomyositis Adult T-Cell Leukemia Agammaglobulinemia Aggressive Periodontitis Aging Aicardi-Goutieres Syndrome Al Amyloidosis Aland Island Eye Disease Albinism-Deafness Syndrome Alexithymia Allergic Asthma Allergic Contact Dermatitis Allergic Encephalomyelitis Allergic Rhinitis Alopecia Alopecia Areata Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alopecia Totalis Alpha-1-Antitrypsin Deficiency Alpha-Fetoprotein Deficiency Alpha-Thalassemia Alport Syndrome, X-Linked Al-Raqad Syndrome Amebiasis Amelogenesis Imperfecta Hypomaturation Type Amyloidosis Amyloidosis Beta2m Anaplastic Large Cell Lymphoma Anemia, Autoimmune Hemolytic Aneurysm Angioedema Angioimmunoblastic T-Cell Lymphoma Anhidrosis Aniridia 1 Annular Erythema Anorexia Nervosa 1 Anterior Scleritis Anterior Uveitis Anti-P200 Pemphigoid Antiphospholipid Syndrome Antisynthetase Syndrome Anuria Aortic Aneurysm Aortitis Aplasia of Lacrimal and Salivary Glands Aplastic Anemia Appendicitis Apple Allergy Aregenerative Anemia Artemis Deficiency Arteries, Anomalies of Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Asbestos Intoxication Asbestosis Ascaris Lumbricoides Infection Aspergillosis Asplenia, Isolated Congenital Asthma Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia - Hypogonadism - Choroidal Dystrophy Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Ataxia-Telangiectasia Athabaskan Brainstem Dysgenesis Syndrome Atherosclerosis Susceptibility Athyreosis Atrial Fibrillation Atrioventricular Block Atrophic Gastritis Attention Deficit-Hyperactivity Disorder Autism Autism Spectrum Disorder Autoimmune Addison Disease Autoimmune Atrophic Gastritis Autoimmune Autonomic Ganglionopathy Autoimmune Disease Autoimmune Disease 2 Autoimmune Disease 3 Autoimmune Disease, Multisystem, with Facial Dysmorphism Autoimmune Disease of Endocrine System Autoimmune Encephalitis Autoimmune Enteropathy Autoimmune Gastrointestinal Dysmotility Autoimmune Hemolytic Anemia, Warm Type Autoimmune Hepatitis Autoimmune Hypoparathyroidism Autoimmune Inner Ear Disease Autoimmune Lymphoproliferative Syndrome Autoimmune Lymphoproliferative Syndrome, Type Iia Autoimmune Lymphoproliferative Syndrome, Type Iii Autoimmune Lymphoproliferative Syndrome, Type V Autoimmune Myocarditis Autoimmune Neuropathy Autoimmune Oophoritis Autoimmune Pancreatitis Autoimmune Pancreatitis Type 1 Autoimmune Pancreatitis Type 2 Autoimmune Polyendocrine Syndrome Autoimmune Polyendocrine Syndrome Type 1 Autoimmune Polyendocrine Syndrome, Type Ii Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia Autoimmune Polyendocrinopathy Type 3 Autoimmune Polyendocrinopathy Type 4 Autoimmune Polyglandular Syndrome Type 3 Autoimmune Progesterone Dermatitis Autoimmune-Related Retinopathy and Optic Neuropathy Autoimmune Retinopathy Autoinflammation with Arthritis and Dyskeratosis Autoinflammation with Infantile Enterocolitis Autonomic Dysfunction Autonomic Neuropathy Babesiosis Bacteriuria Banti's Syndrome Basal Cell Carcinoma Baylisascariasis B Cell Deficiency B-Cell Expansion with Nfkb and T-Cell Anergy B-Cell Lymphomas B Cell Prolymphocytic Leukemia Benign Idiopathic Neonatal Seizures Benign Struma Ovarii Bernard-Soulier Syndrome Beryllium Disease Beta-Thalassemia Bile Duct Disease Biliary Atresia Bipolar Disorder Blackwater Fever Bladder Cancer Blastic Plasmacytoid Dendritic Cell Blau Syndrome Bleeding Disorder, Platelet-Type, 11 Blepharitis Blepharospasm Blood Group--Ahonen Blood Group, Dombrock System Blood Group, Gerbich System Blood Group, I System 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 Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brain Injury Breast Adenocarcinoma Breast Cancer Breast Disease Brittle Diabetes Bronchiolitis Bronchiolitis Obliterans Brucellosis Budd-Chiari Syndrome Bulimia Nervosa 1 Bullous Pemphigoid Bullous Skin Disease Burkitt Lymphoma Burns C1 Inhibitor Deficiency C1q Deficiency Calcinosis Calciphylaxis Cancer-Associated Retinopathy Candidiasis Capillary Leak Syndrome Carboxypeptidase N Deficiency Carcinoid Syndrome Carcinoid Tumors, Intestinal Cardiac Arrest Cardiac Arrhythmia Cardiac Tamponade Cartilage-Hair Hypoplasia Castleman Disease Cataract Cataract 40 Cataract Congenital Dominant Non Nuclear Cataract, Total Congenital Catastrophic Antiphospholipid Syndrome Cat-Scratch Disease Celiac Disease 1 Central Nervous System Disease Central Nervous System Lymphoma Central Nervous System Origin Vertigo Central Nervous System Vasculitis Central Precocious Puberty Cerebellar Degeneration Cerebellar Degeneration-Related Autoantigen 3 Cerebral Atrophy Cerebral Folate Deficiency Cerebritis Cerebrovascular Disease Cervicitis Chagas Disease Chickenpox Chikungunya Chlamydia Cholangiocarcinoma Cholangitis Cholecystitis Cholera Cholestasis Chondroblastoma Chondrodysplasia Punctata Syndrome Chondrosarcoma Chops Syndrome Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chorioretinitis Choroiditis Chromosomal Triplication Chromosome 10p Duplication Chromosome 18p Deletion Syndrome Chromosome 18q Deletion Syndrome Chromosome 2q Deletion Chromosome 4q Deletion Chromosome 5q Deletion Syndrome Chronic Active Epstein-Barr Virus Infection Chronic Beryllium Disease Chronic Eosinophilic Leukemia Chronic Eosinophilic Pneumonia Chronic Fatigue Syndrome Chronic Graft Versus Host Disease Chronic Granulomatous Disease Chronic Inflammatory Demyelinating Polyneuropathy Chronic Inflammatory Demyelinating Polyradiculoneuropathy Chronic Mucocutaneous Candidiasis Chronic Myelomonocytic Leukemia Chronic Pain Chronic Pyelonephritis Chronic Rhinitis Churg-Strauss Syndrome Cicatricial Pemphigoid Cleft Larynx, Posterior Cocoon Syndrome Cogan Syndrome Cohen-Gibson Syndrome Cold Agglutinin Disease Cold Urticaria Colitis Collagen Disease Collagenopathy Type 2 Alpha 1 Collagenous Colitis Colon Adenoma Colorblindness, Partial, Deutan Series Colorblindness, Partial, Protan Series Colorectal Cancer Common Variable Immunodeficiency Complement Component 2 Deficiency Complement Component 3 Deficiency Complement Component 3 Deficiency, Autosomal Recessive Complement Component 4, Partial Deficiency of Complement Component C1s Deficiency Complement Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complex Regional Pain Syndrome Composite Lymphoma Congenital Bile Acid Synthesis Defect Congenital Disorder of Glycosylation, Type Iic Congenital Hemolytic Anemia Congenital Hypothyroidism Congenital Myasthenic Syndrome Congenital Rubella Congenital Stationary Night Blindness Conjunctivitis Conjunctivochalasis Connective Tissue Disease Constricting Bands, Congenital Constrictive Pericarditis Contact Dermatitis Coronary Restenosis Cranioectodermal Dysplasia 1 Crescentic Glomerulonephritis Crest Syndrome Creutzfeldt-Jakob Disease Critical Illness Polyneuropathy Cryoglobulinemia Cryptococcal Meningitis Cryptococcosis Culler-Jones Syndrome Cutaneous Candidiasis Cutaneous Leishmaniasis Cutaneous Polyarteritis Nodosa Cutaneous Sclerosis Cutis Marmorata Telangiectatica Congenita Cyclic Vomiting Syndrome Cystic Echinococcosis Cystic Fibrosis Cystitis Cytochrome P450 2d6 Variant Cytomegalic Inclusion Disease Cytomegalovirus Infection Cytomegalovirus Retinitis Cytophagic Histiocytic Panniculitis Dacryoadenitis Dacryocystitis Danubian Endemic Familial Nephropathy Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Degenerative Disc Disease Dementia Demyelinating Disease Demyelinating Polyneuropathy Dermatitis Dermatitis Herpetiformis Dermatomyositis Dermoid Cyst Desquamative Interstitial Pneumonia Diabetes Insipidus Diabetes Mellitus Diabetes Mellitus, Insulin-Dependent Diabetes Mellitus, Ketosis-Prone Diabetic Angiopathy Diabetic Autonomic Neuropathy Diarrhea Diastolic Heart Failure Diffuse Alveolar Hemorrhage Diffuse Large B-Cell Lymphoma Digeorge Syndrome Dilated Cardiomyopathy Diphtheria Discoid Lupus Erythematosus Disseminated Intravascular Coagulation Down Syndrome Drug-Induced Autoimmune Hemolytic Anemia Drug-Induced Hepatitis Drug Rash with Eosinophilia and Systemic Symptoms Duodenal Ulcer Duodenitis Dysautonomia Dysfibrinogenemia Dysgammaglobulinemia Dyskeratosis Congenita Dysphagia Dystonia Echinococcosis Eclampsia Ectodermal Dysplasia Emery-Dreifuss Muscular Dystrophy Empty Sella Syndrome Encephalitis Encephalopathy Endemic Goiter Endocarditis Endocrine Exophthalmos Endogenous Depression Endometriosis Endometritis Endotheliitis End Stage Renal Failure Enterocolitis Enteropathica Enteropathy-Associated T-Cell Lymphoma Eosinophilic Colitis Eosinophilic Fasciitis Eosinophilic Granulomatosis with Polyangiitis Eosinophilic Pneumonia Epidermolysis Bullosa Epidermolysis Bullosa Acquisita Epididymo-Orchitis Epilepsy Episodic Ataxia Episodic Ataxia, Type 1 Epithelial Recurrent Erosion Dystrophy Erythema Elevatum Diutinum Erythema Multiforme Erythromelalgia Eustachian Tube Disease Evans' Syndrome Exocrine Pancreatic Insufficiency Exophthalmos Fabry Disease Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature Factor Viii Deficiency Factor Xiii Deficiency Familial Mediterranean Fever Familial Thyroid Dyshormonogenesis Fanconi Anemia, Complementation Group E Fanconi Renotubular Syndrome 1 Fanconi Syndrome Far Eastern Spotted Fever Fasciitis Fascioliasis Fatty Liver Disease Febrile Infection-Related Epilepsy Syndrome Fibrillary Glomerulonephritis Fibrocalculous Pancreatopathy Fibromatosis, Gingival, 2 Fibrosclerosis, Multifocal Fibrous Histiocytoma Fibular Hypoplasia and Complex Brachydactyly Filariasis Focal Dystonia Focal Epilepsy Focal Segmental Glomerulosclerosis Follicular Adenoma Folliculotropic Mycosis Fungoides Food Allergy Fragile X Syndrome Friedreich Ataxia 1 Frontotemporal Dementia Fundus Albipunctatus Galactose Epimerase Deficiency Gamma Heavy Chain Disease Gastric Cancer Gastric Lymphoma Gastric Ulcer Gastritis Gastritis, Familial Giant Hypertrophic Gastrointestinal Stromal Tumor Generalized Resistance to Thyroid Hormone Genitopatellar Syndrome Gestational Diabetes Giant Cell Myocarditis Gigantomastia Gingival Hypertrophy Gingivitis Glaucoma-Related Pigment Dispersion Syndrome Glioblastoma Glioblastoma Multiforme Glioma Glomerulonephritis Glossodynia Glossopharyngeal Neuralgia Glucocorticoid-Induced Osteoporosis Glucocorticoid Resistance, Generalized Glucose/galactose Malabsorption Glucose Intolerance Glycogen Storage Disease Goiter Goiter, Multinodular 1, with or Without Sertoli-Leydig Cell Tumors Goodpasture Syndrome Good Syndrome Graft-Versus-Host Disease Granulocytopenia Granuloma Annulare Granulomatous Dermatitis Granulomatous Mastitis Graves' Disease Graves Disease 1 Gray Platelet Syndrome Growth Hormone Deficiency Hairy Cell Leukemia Hansen's Disease Harlequin Syndrome Hashimoto's Encephalitis Hashimoto Thyroiditis Headache Heavy Chain Disease Helicobacter Pylori Infection Hellp Syndrome Hemangioma Hematopoietic Stem Cell Transplantation Hemochromatosis, Neonatal Hemoglobin C Disease Hemoglobinemia Hemoglobinuria Hemolytic Anemia Hemolytic Anemia, Cd59-Mediated, with or Without Immune-Mediated Polyneuropathy Hemolytic-Uremic Syndrome Hemophagocytic Lymphohistiocytosis Hemophilia Hemophilia a Henoch-Schoenlein Purpura Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis E Hepatocellular Carcinoma Hepatopulmonary Syndrome Hepatosplenic T-Cell Lymphoma Hereditary Angioedema Hereditary Spherocytosis Herpes Gestationis Herpes Simplex Herpes Simplex Encephalitis Herpes Zoster Herpetiform Pemphigus Hidradenitis Hidradenitis Suppurativa Histiocytic Sarcoma Histiocytoma Histiocytosis Histiocytosis-Lymphadenopathy Plus Syndrome Human Coronavirus Sensitivity Human Herpesvirus 8 Human Immunodeficiency Virus Type 1 Human T-Cell Leukemia Virus Type 1 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant Hypercholesterolemia, Autosomal Dominant, 3 Hypereosinophilic Syndrome Hyper Ige Syndrome Hyperinsulinemic Hypoglycemia Hyperlucent Lung Hyperparathyroidism Hyperproinsulinemia Hyperprolactinemia Hypersensitivity Reaction Disease Hypersensitivity Reaction Type Iii Disease Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hyperthyroxinemia Hypertrichosis Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypoadrenalism Hypoadrenocorticism, Familial Hypoglycemia Hypoglycemic Coma Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypoparathyroidism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypopituitarism Hypopyon Hypothyroidism Hypothyroidism, Congenital, Nongoitrous, 2 Hypothyroidism, Congenital, Nongoitrous, 4 Hypothyroidism, Thyroidal or Athyroidal, with Spiky Hair and Cleft Palate Hypotrichosis 1 Hypoxia Ichthyosis Ichthyosis Prematurity Syndrome Idiopathic Achalasia Idiopathic Bilateral Vestibulopathy Idiopathic Hypertrophic Pachymeningitis Idiopathic Inflammatory Myopathy Idiopathic Neutropenia Idiopathic Recurrent Pericarditis Ige Responsiveness, Atopic Igg4-Related Dacryoadenitis and Sialadenitis Igg4-Related Disease Igg4-Related Hepatopathy Igg4-Related Pachymeningitis Igg4-Related Sclerosing Cholangitis Ileitis Immune-Complex Glomerulonephritis Immune Deficiency Disease Immune Suppression Immunodeficiency 20 Immunodeficiency 43 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked Immunoglobulin a Deficiency 1 Immunoglobulin Alpha Deficiency Immunoglobulin E Concentration, Serum Inclusion Body Myositis Infective Endocarditis Infertility Inflammatory Bowel Disease Inflammatory Myofibroblastic Tumor Influenza Inguinal Hernia Inner Ear Disease Insulin Autoimmune Syndrome Insulin-Like Growth Factor I Insulinoma Intermediate Uveitis Interstitial Cystitis Interstitial Lung Disease Interstitial Nephritis Intestinal Benign Neoplasm Intestinal Disease Intestinal Perforation Intestinal Pseudo-Obstruction Intestinal Tuberculosis Intrahepatic Cholangiocarcinoma Intrahepatic Cholestasis Invasive Aspergillosis Iridocyclitis Iritis Ischemic Optic Neuropathy Isolated Gonadotropin-Releasing Hormone Deficiency Itch E3 Ubiquitin Ligase Deficiency Japanese Encephalitis Juvenile Rheumatoid Arthritis Kallmann Syndrome Kaposi Sarcoma Kawasaki Disease Kearns-Sayre Syndrome Keratoconjunctivitis Keratoconjunctivitis Sicca Keratopathy Keratosis Keshan Disease Kikuchi Disease Kleine-Levin Hibernation Syndrome Kniest Dysplasia Labyrinthitis Lambert-Eaton Myasthenic Syndrome Lambert Syndrome Landau-Kleffner Syndrome Langerhans Cell Histiocytosis Large Cell Neuroendocrine Carcinoma Large Granular Lymphocyte Leukemia Laryngeal Adductor Paralysis Laryngeal Cleft Lateral Sclerosis Leiomyosarcoma Leishmaniasis Leprosy 3 Leptospirosis Leukemia Leukodystrophy Leukodystrophy, Hypomyelinating, 5 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lichen Amyloidosis Lichen Planopilaris Lichen Planus Lichen Sclerosus Li-Fraumeni Syndrome Li-Fraumeni Syndrome 2 Limbal Stem Cell Deficiency Limbic Encephalitis Linear Iga Disease Linear Scleroderma Lipodystrophy Lipoprotein Glomerulopathy Lissencephaly 1 Listeriosis Liver Cirrhosis Liver Disease Liver Inflammatory Pseudotumor Localized Scleroderma Long Qt Syndrome Lubs X-Linked Mental Retardation Syndrome Lung Cancer Lung Disease Lung Large Cell Carcinoma Lung Papillary Adenocarcinoma Lupus Erythematosus Lupus Erythematosus Panniculitis Lyme Disease Lymphadenitis Lymphangiectasia, Intestinal Lymphoblastic Leukemia Lymphocytic Choriomeningitis Lymphocytic Colitis Lymphocytic Hypophysitis Lymphoepithelioma-Like Thymic Carcinoma Lymphogranuloma Venereum Lymphoma Lymphoma, Mucosa-Associated Lymphoid Type Lymphopenia Lymphoproliferative Syndrome Lymphoproliferative Syndrome, X-Linked, 1 Lysosomal Storage Disease Macrocytic Anemia Macroglobulinemia Macrophage Activation Syndrome Macrophagic Myofasciitis Malakoplakia Malaria Male Infertility Malignant Histiocytosis Malignant Hypertension Malignant Peritoneal Mesothelioma Malignant Spiradenoma Marden-Walker Syndrome Mastitis Maturity-Onset Diabetes of the Young Mccune-Albright Syndrome Measles Meckel Syndrome, Type 1 Med23 Mediastinitis Meester-Loeys Syndrome Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 Melanoma Melanoma-Associated Retinopathy Melkersson-Rosenthal Syndrome Membranoproliferative Glomerulonephritis Membranous Nephropathy Meningitis Meningococcal Meningitis Meningoencephalitis Menkes Disease Merkel Cell Carcinoma Metabolic Acidosis Metachromatic Leukodystrophy Methemoglobinemia Methotrexate-Associated Lymphoproliferative Disorders Microinvasive Gastric Cancer Microphthalmia, Syndromic 1 Microscopic Polyangiitis Mid-Dermal Elastolysis Middle Ear Disease Migraine with or Without Aura 1 Mikulicz Disease Miliary Tuberculosis Miller Fisher Syndrome Mitochondrial Dna Depletion Syndrome 4a Mixed Connective Tissue Disease Mixed-Type Autoimmune Hemolytic Anemia Miyoshi Muscular Dystrophy 1 Monocarboxylate Transporter 1 Deficiency Monocytic Leukemia Mood Disorder Morbid Obesity Motor Neuron Disease Mowat-Wilson Syndrome Mucinoses Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Vii Mucositis Multicentric Castleman Disease Multicentric Reticulohistiocytosis Multifocal Motor Neuropathy Multinodular Goiter Multiple Endocrine Neoplasia Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Pterygium Syndrome, Lethal Type Multiple Sclerosis Multiple System Atrophy 1 Mumps Muscle Disorders Muscular Atrophy Muscular Dystrophy Musical Perfect Pitch Myasthenia Gravis Mycobacterium Tuberculosis 1 Mycosis Fungoides Myelitis Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloid Sarcoma Myeloma, Multiple Myhre Syndrome Myocardial Infarction Myocarditis Myoclonic Astatic Epilepsy Myoclonic Epilepsy of Infancy Myoclonus Myopathy Myopathy, Tubular Aggregate, 1 Myositis Myotonia Myotonic Dystrophy Myxedema Myxoid Chondrosarcoma Nail Disease Narcolepsy Necrobiosis Lipoidica Necrotizing Autoimmune Myopathy Neonatal Hypothyroidism Neonatal Systemic Lupus Erythematosus Neonatal Thyrotoxicosis Nephrotic Syndrome Nervous System Disease Neuraminidase Deficiency Neuritis Neuroaxonal Dystrophy Neuroblastoma Neuroendocrine Tumor Neuromuscular Disease Neuromyelitis Optica Neuromyelitis Optica Spectrum Disorder Neuronitis Neuropathy Neuropathy, Hereditary Sensory and Autonomic, Type Iia Neuropathy, Hereditary Sensory and Autonomic, Type Iii Neurosarcoidosis Neurosyphilis Neutropenia Neutrophilic Dermatosis, Acute Febrile Night Blindness Nijmegen Breakage Syndrome Nocardiosis Nodding Syndrome Nodular Goiter Nodular Lymphocyte Predominant Hodgkin Lymphoma Nodular Regenerative Hyperplasia Nonalcoholic Steatohepatitis Nonspecific Interstitial Pneumonia Nontoxic Goiter Noonan Syndrome 3 Norse Obsessive-Compulsive Disorder Obstructive Jaundice Occipital Horn Syndrome Ocular Cicatricial Pemphigoid Ocular Hypertension Ocular Melanoma Ocular Motor Apraxia Oligoastrocytoma Omenn Syndrome Onchocerciasis Opitz Gbbb Syndrome, Type I Opportunistic Mycosis Opsoclonus-Myoclonus Syndrome Optic Neuritis Oral Candidiasis Oral Lichen Planus Oral Squamous Cell Carcinoma Orbital Plasma Cell Granuloma Orchitis Osseous Heteroplasia, Progressive Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteomyelitis Osteonecrosis Osteonecrosis of the Jaw Osteosclerotic Myeloma Otitis Media Otosclerosis Ovalocytosis, Southeast Asian Ovarian Cancer Ovarian Cyst Ovarian Disease Ovarian Hyperstimulation Syndrome Ovarian Lymphoma Overhydrated Hereditary Stomatocytosis Paine Syndrome Pancreas, Annular Pancreatic Agenesis 1 Pancreatic Cancer Pancreatic Ductal Adenocarcinoma Pancreatitis Pancytopenia Pandas Panniculitis Panuveitis Papillary Adenocarcinoma Papillary Carcinoma Papilloma Papillomatosis, Confluent and Reticulated Papillon-Lefevre Syndrome Paracoccidioidomycosis Paranasal Sinus Disease Paraneoplastic Cerebellar Degeneration Paraneoplastic Pemphigus Paraneoplastic Syndromes Paranoid Schizophrenia Parathyroid Carcinoma Parotitis Paroxysmal Nocturnal Hemoglobinuria Pars Planitis Pdgfrb-Associated Chronic Eosinophilic Leukemia Pediatric Multiple Sclerosis Pediatric Systemic Lupus Erythematosus Pediatric Ulcerative Colitis Pemphigoid Gestationis Pemphigus Pemphigus Erythematosus Pemphigus Foliaceus Pemphigus Vegetans Pemphigus Vulgaris Pendred Syndrome Pericardial Effusion Pericarditis Pericholangitis Perilymphatic Fistula Periodontal Disease Periodontitis Peripartum Cardiomyopathy Peripheral Nervous System Disease Peripheral T-Cell Lymphoma Peritoneal Mesothelioma Peritonitis Pernicious Anemia Persian Gulf Syndrome Pertussis Pfeiffer Syndrome Pheochromocytoma Pigmented Basal Cell Carcinoma Pilonidal Sinus Pitt-Hopkins Syndrome Pituitary Adenoma Pityriasis Lichenoides Pityriasis Lichenoides Chronica Pityriasis Rosea Pityriasis Rubra Pilaris Plasmodium Vivax Malaria Pleomorphic Rhabdomyosarcoma Pleurisy Plummer's Disease Pneumonia Poems Syndrome Polyarteritis Nodosa Polyclonal Hypergammaglobulinemia Polycystic Ovary Syndrome Polydactyly, Postaxial, with Progressive Myopia Polymicrogyria Polymicrogyria, Bilateral Perisylvian, X-Linked Polymorphic Reticulosis Polymyositis Polyneuropathy Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes Polyradiculoneuropathy Porphyria Porphyria Cutanea Tarda Portal Hypertension Portal Vein Thrombosis Posterior Uveitis Postorgasmic Illness Syndrome Postpartum Depression Postpartum Psychosis Post-Transplant Lymphoproliferative Disease Postural Orthostatic Tachycardia Syndrome Potocki-Lupski Syndrome Pouchitis Precocious Puberty Prediabetes Syndrome Pre-Eclampsia Premature Menopause Premature Ovarian Failure 1 Premature Ovarian Failure 7 Prieto X-Linked Mental Retardation Syndrome Primary Agammaglobulinemia Primary Anetoderma Primary Bacterial Infectious Disease Primary Biliary Cholangitis Primary Biliary Cirrhosis Primary Effusion Lymphoma Primary Hyperparathyroidism Primary Intestinal Lymphangiectasia Primary Lateral Sclerosis, Adult, 1 Primary Systemic Mycosis Proctitis Progressive Multifocal Leukoencephalopathy Progressive Muscular Atrophy Proliferative Glomerulonephritis Prolymphocytic Leukemia Properdin Deficiency, X-Linked Prostate Cancer Prostatitis Protein C Deficiency Protein-Losing Enteropathy Protein S Deficiency Protein Z Deficiency Prurigo Nodularis Psoriasis Psoriasis 13 Psoriatic Arthritis Psychotic Disorder Pten Hamartoma Tumor Syndrome Pulmonary Alveolar Microlithiasis Pulmonary Alveolar Proteinosis Pulmonary Alveolar Proteinosis, Acquired Pulmonary Disease, Chronic Obstructive Pulmonary Embolism Pulmonary Fibrosis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hypertension Pulmonary Hypertension, Primary, 1 Pulmonary Plasma Cell Granuloma Pulmonary Sarcoidosis Pulmonary Tuberculosis Pure Red-Cell Aplasia Purine Nucleoside Phosphorylase Deficiency Purpura Purpura Fulminans Pustular Psoriasis Pyelonephritis Pyoderma Pyoderma Gangrenosum Pyomyositis Q Fever Rabies Rapidly Progressive Glomerulonephritis Rapp-Hodgkin Syndrome Ras-Associated Autoimmune Leukoproliferative Disorder Rasmussen Encephalitis Reactive Arthritis Refractory Anemia Refractory Celiac Disease Relapsing Polychondritis Relapsing-Remitting Multiple Sclerosis Rem Sleep Behavior Disorder Renal Glucosuria Renal Tubular Acidosis Retinal Degeneration Retinal Detachment Retinal Disease Retinal Vasculitis Retinitis Retinitis Pigmentosa and Erythrocytic Microcytosis Retinoblastoma Retroperitoneal Fibrosis Rhabdomyosarcoma Rheumatic Disease Rheumatic Fever Rheumatic Fever-Related Antigen Rheumatic Heart Disease Rheumatoid Arthritis Rhinitis Riddle Syndrome Rift Valley Fever Ring Chromosome 18 Ringed Hair Rippling Muscle Disease 2 Rosai-Dorfman Disease Rubella Sacrococcygeal Teratoma Sakati Syndrome Salivary Gland Adenoma, Pleomorphic Salpingitis Salt and Pepper Developmental Regression Syndrome Sarcoidosis 2 Sarcoma Satb2-Associated Syndrome Schimke Immunoosseous Dysplasia Schimmelpenning-Feuerstein-Mims Syndrome Schistosomiasis Schizoaffective Disorder Schizophrenia Schnitzler Syndrome Scleritis Scleromyxedema Sclerosing Cholangitis Scrapie Sea-Blue Histiocyte Disease Secondary Adrenal Insufficiency Secondary Pulmonary Alveolar Proteinosis Secondary Syphilis Seizures, Benign Familial Neonatal, 1 Sensorineural Hearing Loss Severe Combined Immunodeficiency Severe Combined Immunodeficiency, X-Linked Severe Congenital Neutropenia Shwachman-Diamond Syndrome Sialadenitis Sick Building Syndrome Sickle Cell Anemia Sickle Cell Disease Sideroblastic Anemia Silicosis Sjogren Syndrome Skeletal Dysplasias Skin Disease Sleep Apnea Sleep Disorder Smallpox Smith-Magenis Syndrome Somatoform Disorder Spasmodic Dysphonia Spastic Ataxia, Charlevoix-Saguenay Type Spastic Cerebral Palsy Spasticity Spastic Paraparesis Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinal Cord Injury Splenic Disease Splenic Infarction Splenic Marginal Zone Lymphoma Splenomegaly Spondylarthropathy Spondylitis Spondyloarthropathy Spondyloarthropathy 1 Spondylocarpotarsal Synostosis Syndrome Spondyloenchondrodysplasia Spondyloenchondrodysplasia with Immune Dysregulation Sporotrichosis Squamous Cell Carcinoma Status Epilepticus Steatocystoma Multiplex Steatorrhea Stiff-Person Syndrome Stomach Disease Stomatitis Strabismus Streptococcal Group a Invasive Disease Struma Ovarii Subacute Lymphocytic Thyroiditis Subacute Thyroiditis Sudden Infant Death Syndrome Sudden Sensorineural Hearing Loss Suppressor of Tumorigenicity 3 Surfactant Metabolism Dysfunction, Pulmonary, 2 Surfactant Metabolism Dysfunction, Pulmonary, 3 Surfactant Metabolism Dysfunction, Pulmonary, 4 Susac Syndrome Sveinsson Chorioretinal Atrophy Swallowing Disorders Sydenham Chorea Sympathetic Ophthalmia Syndrome of Inappropriate Antidiuretic Hormone Synovitis Syphilis Syringoma Systemic Capillary Leak Syndrome Systemic Lupus Erythematosus Systemic Mastocytosis Systemic Onset Juvenile Idiopathic Arthritis Systemic Polyarteritis Nodosa T Cell Deficiency T-Cell/histiocyte Rich Large B Cell Lymphoma T-Cell Immunodeficiency, Recurrent Infections, and Autoimmunity with or Without Cardiac Malformations T-Cell Leukemia T-Cell Prolymphocytic Leukemia Telangiectasia, Hereditary Benign Temporal Lobe Epilepsy Teratoma Testicular Regression Syndrome Testicular Torsion Tetanus Tetragametic Chimerism Thalassemia Third-Degree Atrioventricular Block Thrombasthenia Thrombocytopenia Thrombocytopenia 1 Thrombocytopenic Purpura, Autoimmune Thrombocytosis Thrombophilia Thrombosis Thrombotic Thrombocytopenic Purpura Thymic Dysplasia Thymic Hyperplasia Thymoma Thyroid Cancer Thyroid Cancer, Nonmedullary, 1 Thyroid Cancer, Nonmedullary, 2 Thyroid Gland Disease Thyroiditis Thyroid Lymphoma Tic Disorder Tinea Pedis Tolosa-Hunt Syndrome Tonsillitis Toxic Diffuse Goiter Toxic Oil Syndrome Toxoplasmoză Tracheal Stenosis Trachoma Transverse Myelitis Traumatic Brain Injury Treacher Collins Syndrome 1 Trichothiodystrophy 4, Nonphotosensitive Triple X Syndrome Tropical Spastic Paraparesis Turner Syndrome Tympanosclerosis Type 1 Diabetes Mellitus 11 Type 1 Diabetes Mellitus 12 Type 1 Diabetes Mellitus 13 Type 1 Diabetes Mellitus 17 Type 1 Diabetes Mellitus 2 Type 1 Diabetes Mellitus 5 Type Ii Mixed Cryoglobulinemia Ulcerative Colitis Ulcerative Stomatitis Undifferentiated Connective Tissue Disease Urinary Schistosomiasis Urticaria Usher Syndrome Uveitis Vaccinia Valproate Embryopathy Van Der Woude Syndrome 1 Vascular Hemostatic Disease Vasculitis Velocardiofacial Syndrome Ventricular Septal Defect Vernal Keratoconjunctivitis Viral Hepatitis Visceral Leishmaniasis Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Vogt-Koyanagi-Harada Disease Vulvitis Vulvovaginitis Waterhouse-Friderichsen Syndrome Wegener Granulomatosis Whipple Disease Wild Type Attr Amyloidosis Williams-Beuren Syndrome Wiskott-Aldrich Syndrome Wolfram Syndrome Xerophthalmia X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome Yellow Fever Zollinger-Ellison Syndrome