Informaţii despre

Nume Neutropenia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Agranulocytosis
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge; Boli nefrologice (ale rinichilor); Boli osoase
Boli din aceeaşi familie Neutropenia, Chronic Familial; Neutropenia, Severe Congenital, 1, Autosomal Dominant; Neutropenia, Severe Congenital, 2, Autosomal Dominant; Neutropenia, Severe Congenital, 3, Autosomal Recessive; Neutropenia, Severe Congenital, 4, Autosomal Recessive; Neutropenia, Severe Congenital, 5, Autosomal Recessive; Neutropenia, Severe Congenital, 6, Autosomal Recessive; Neutropenia, Severe Congenital, 7, Autosomal Recessive; Severe Congenital Neutropenia; Severe Congenital Neutropenia Autosomal Dominant

Vezi şi

Boli A-Z 3-Methylglutaconic Aciduria Ablepharon-Macrostomia Syndrome Acquired Immunodeficiency Syndrome Acrocallosal Syndrome Acute Graft Versus Host Disease Acute Leukemia Acute Lymphocytic Leukemia Acute Respiratory Distress Syndrome Adenosine Deaminase Deficiency Agammaglobulinemia Aging Albinism Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Anauxetic Dysplasia 1 Anca-Associated Vasculitis Anemia of Prematurity Aneurysm Aniridia 1 Anorexia Nervosa 1 Aphthous Stomatitis Aplastic Anemia Appendicitis Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 5 Arthropathy Aspergillosis Autoimmune Disease Autoimmune Hepatitis Autoimmune Pancreatitis Autoinflammation with Infantile Enterocolitis Babesiosis Barth Syndrome B-Cell Expansion with Nfkb and T-Cell Anergy B-Cell Lymphomas Beta-Lactam Allergy Bleeding Disorder, Platelet-Type, 11 Blepharitis Blood Group--Ahonen Blood Group, Dombrock 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 Edema Brain Injury Breast Cancer Breast Cancer-Related Regulator of Tp53 Bullous Pemphigoid Calcinosis Candidiasis Cardiomyopathy, Dilated, 3b Cartilage-Hair Hypoplasia Cataract Cd40 Ligand Deficiency Celiac Disease 1 Cellulitis Centronuclear Myopathy Cerebellar Atrophy, Developmental Delay, and Seizures Cerebellar Degeneration Cerebral Artery Occlusion Cerebritis Cervicitis Chancroid Chediak-Higashi Syndrome Cheilitis Childhood-Onset Schizophrenia Chlamydia Chops Syndrome Choriocarcinoma Chromosomal Triplication Chronic Graft Versus Host Disease Chronic Granulomatous Disease Chronic Myelomonocytic Leukemia Chronic Neutrophilic Leukemia Chronic Orbital Inflammation Chronic Pyelonephritis Cicatricial Pemphigoid Clostridium Septicum Infection Cocaine Abuse Cohen Syndrome Colitis Colorectal Cancer Common Variable Immunodeficiency Complement Component 9 Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Cytomegalovirus Congenital Disorder of Glycosylation, Type Iic Corneal Dystrophy, Avellino Type Coronary Artery Aneurysm Coronary Stenosis Cote Katsantoni Syndrome Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Crohn's Colitis Crohn's Disease Cryptococcosis Cryptogenic Organizing Pneumonia Cyclic Neutropenia Cytomegalovirus Infection Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Demyelinating Disease Dengue Hemorrhagic Fever Dermatophytosis Diarrhea Diffuse Large B-Cell Lymphoma Dihydropyrimidine Dehydrogenase Deficiency Dilated Cardiomyopathy Duane Retraction Syndrome 1 Dwarfism Dysgammaglobulinemia Dyskeratosis Congenita Dysostosis Ecthyma Ectodermal Dysplasia Ehrlichiosis Elane-Related Neutropenia Encephalitis Endophthalmitis Endotheliitis Engraftment Syndrome Enterocolitis Eosinophilic Fasciitis Epididymo-Orchitis Epiglottitis Epilepsy Epulis Erysipelas Erythema Multiforme Esophageal Cancer Essential Thrombocythemia Ewing Sarcoma Exocrine Pancreatic Insufficiency Familial Mediterranean Fever Fasciitis Felty Syndrome Female Breast Cancer Fusariosis G6pc3 Deficiency Gas Gangrene Gastric Cancer Gastritis Gastrointestinal Stromal Tumor Germ Cells Tumors Gingivitis Glioblastoma Glomerulonephritis Glucose/galactose Malabsorption Glycogen Storage Disease Glycogen Storage Disease Ib Graft-Versus-Host Disease Granulocytopenia Granulomatous Hepatitis Hairy Cell Leukemia Helicobacter Pylori Infection Hemangioendothelioma Hematopoietic Stem Cell Transplantation Hemoglobinuria Hemolytic Anemia Hemorrhagic Fever Hepatic Adenomas, Familial Hepatitis Hepatitis C Hepatitis C Virus Herpes Simplex Herpes Simplex Encephalitis Herpes Zoster Hinman Syndrome Histiocytosis Human Coronavirus Sensitivity Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperglycemia Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypertrophic Cardiomyopathy Idiopathic Neutropenia Ileocolitis Immune Deficiency Disease Inflammatory Bowel Disease 1 Influenza Invasive Aspergillosis Invasive Mole Kawasaki Disease Lambert-Eaton Myasthenic Syndrome Lambert Syndrome Large Granular Lymphocyte Leukemia Laryngitis Leukemia Leukemia, Chronic Myeloid Leukocyte Disease Light Fixation Seizure Syndrome Linear Iga Disease Lung Cancer Lupus Erythematosus Lymphoblastic Leukemia Lymphoma Lymphoma, Mucosa-Associated Lymphoid Type Lymphoma, Non-Hodgkin, Familial Lymphomatoid Granulomatosis Lymphopenia Lymphoproliferative Syndrome, X-Linked, 1 Macular Dystrophy, Retinal, 1, North Carolina Type Malaria Mantle Cell Lymphoma Mastoiditis Melanoma Melioidosis Miliaria Mitochondrial Disorders Miyoshi Muscular Dystrophy 1 Monocytic Leukemia Mucopolysaccharidosis, Type Vii Mucositis Multiple Sclerosis Mungan Syndrome Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloid Sarcoma Myeloma, Multiple Myeloperoxidase Deficiency Myocarditis Myopathy Necrobiotic Xanthogranuloma Necrotizing Soft Tissue Infection Neonatal Alloimmune Neutropenia Nephrotic Syndrome Neuroblastoma Neuromyelitis Optica Neuropathy Neutropenia, Nonimmune Chronic Idiopathic, of Adults Neutropenia, Severe Congenital, 3, Autosomal Recessive Neutropenia, Severe Congenital, 4, Autosomal Recessive Neutropenia, Severe Congenital, X-Linked Neutrophilia, Hereditary Noma Occipital Horn Syndrome Ocular Cicatricial Pemphigoid Oculocutaneous Albinism Ophthalmia Neonatorum Orbital Cellulitis Orbital Plasma Cell Granuloma Orchitis Ovarian Cancer Overhydrated Hereditary Stomatocytosis Pancreatic Cancer Pancreatitis Pancytopenia Paraquat Poisoning Parkinsonism with Spasticity, X-Linked Paronychia Paroxysmal Cold Hemoglobinuria Paroxysmal Nocturnal Hemoglobinuria Pdgfrb-Associated Chronic Eosinophilic Leukemia Periodontal Disease Periodontitis Pfeiffer Syndrome Plasmodium Falciparum Malaria Pneumonia Poikiloderma with Neutropenia Pompholyx Proctitis Properdin Deficiency Properdin Deficiency, X-Linked Propionic Acidemia Prostate Cancer Prostatitis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pure Red-Cell Aplasia Purpura Pustulosis Palmaris Et Plantaris Pyelonephritis Pyoderma Pyoderma Gangrenosum Pyomyositis Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia Rapidly Progressive Glomerulonephritis Rapp-Hodgkin Syndrome Refractory Anemia Relapsing-Remitting Multiple Sclerosis Renpenning Syndrome 1 Retinitis Pigmentosa and Erythrocytic Microcytosis Retinoblastoma Rheumatic Disease Rheumatoid Arthritis Richards-Rundle Syndrome Robinow Syndrome, Autosomal Recessive Rothmund-Thomson Syndrome Sarcoma Schizoaffective Disorder Schizophrenia Sea-Blue Histiocyte Disease Seborrheic Infantile Dermatitis Severe Combined Immunodeficiency Severe Congenital Neutropenia Severe Congenital Neutropenia Autosomal Dominant Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Shwachman-Diamond Syndrome Sickle Cell Disease Small Cell Cancer of the Lung Soft Tissue Sarcoma Spastic Paraplegia 32, Autosomal Recessive Splenic Abscess Splenic Marginal Zone Lymphoma Splenic Tuberculosis Splenomegaly Spondylitis Spondyloarthropathy 1 Spondyloocular Syndrome Squamous Cell Carcinoma Stomatitis Systemic Lupus Erythematosus T Cell Deficiency T-Cell Large Granular Lymphocyte Leukemia Testicular Germ Cell Tumor Testicular Germ Cell Tumor 1 Tetraploidy Three M Syndrome 1 Thrombocytopenia Thrombocytosis Thrombosis Tn Polyagglutination Syndrome Tonsillitis Transient Neonatal Neutropenia Traumatic Brain Injury Ulcerative Proctitis Undifferentiated Pleomorphic Sarcoma Uveitis Vascular Disease Vasculitis Virus Associated Hemophagocytic Syndrome Whim Syndrome Wiskott-Aldrich Syndrome Witkop Syndrome X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome Zinc, Elevated Plasma Zygomycosis