Informaţii despre

Nume Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2
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Boli A-Z Aarskog-Scott Syndrome Achalasia-Addisonianism-Alacrima Syndrome Acquired Amegakaryocytic Thrombocytopenia Acute Leukemia Acute Liver Failure Acute Lymphocytic Leukemia Acute Promyelocytic Leukemia Adenocarcinoma Aging Alopecia Alopecia Totalis Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Alzheimer Disease 3 Anauxetic Dysplasia 1 Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Aplastic Anemia Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aspergillosis Atherosclerosis Susceptibility Autoimmune Disease Autoimmune Lymphoproliferative Syndrome, Type V Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen 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 Marrow Failure Syndrome 1 Bullous Pemphigoid Candidiasis Cd4/cd8 T-Cell Ratio Cerebellar Degeneration-Related Autoantigen 3 Cerebritis Cervical Intraepithelial Neoplasia Chloramphenicol Toxicity Choledocholithiasis Chromosomal Triplication Chronic Graft Versus Host Disease Chronic Mucocutaneous Candidiasis Chronic Myelomonocytic Leukemia Colitis Colorectal Cancer Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Iic Congenital Hypoplastic Anemia Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Cutaneous Sclerosis Cystitis Cytomegalovirus Retinitis Diabetes Mellitus Diamond-Blackfan Anemia Diffuse Scleroderma Disseminated Intravascular Coagulation Down Syndrome Dubowitz Syndrome Dwarfism Dyskeratosis Congenita Dyskeratosis Congenita Autosomal Dominant Dyskeratosis Congenita, Autosomal Dominant 1 Ecthyma Emphysema, Congenital Lobar Encephalitis Encephalopathy Endometriosis Endotheliitis Eosinophilic Fasciitis Epilepsy Essential Thrombocythemia Evans' Syndrome Fasciitis Focal Segmental Glomerulosclerosis Food Allergy Fulminant Viral Hepatitis Fusariosis Gilbert Syndrome Glioblastoma Glioblastoma Multiforme Glycogen Storage Disease Ixc Gout Graft-Versus-Host Disease Granulocytopenia Hairy Cell Leukemia Hematopoietic Stem Cell Transplantation Hemoglobinuria Hemolytic Anemia Hemophagocytic Lymphohistiocytosis Hemorrhagic Cystitis Hemosiderosis Hepatic Adenomas, Familial Hepatitis Hepatitis a Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Hereditary Spherocytosis Histiocytosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypoxia Ichthyosis Prematurity Syndrome Idiopathic Neutropenia Immune Suppression Immunoglobulin E Concentration, Serum Influenza Inherited Bone Marrow Failure Syndromes Interstitial Lung Disease Invasive Aspergillosis Large Granular Lymphocyte Leukemia Leukemia Limbic Encephalitis Long Qt Syndrome Lung Cancer Lung Disease Lupus Erythematosus Lymphoblastic Leukemia Lymphocytic Choriomeningitis Lymphoma Lymphoplasmacytic Lymphoma Megaloblastic Anemia Melanoma Membranous Nephropathy Migraine with or Without Aura 1 Miliary Tuberculosis Miller-Dieker Lissencephaly Syndrome Monocytic Leukemia Mucoepithelial Dysplasia, Hereditary Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Myasthenia Gravis Myelitis Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloperoxidase Deficiency Myositis Myositis Ossificans Necrotizing Fasciitis Nephrotic Syndrome Neutropenia Nijmegen Breakage Syndrome Nodular Regenerative Hyperplasia Non-a-E Hepatitis Non-Involuting Congenital Hemangioma Paine Syndrome Pancreatitis Pancytopenia Panniculitis Papilledema Parainfluenza Virus Type 3 Paroxysmal Nocturnal Hemoglobinuria Pdgfrb-Associated Chronic Eosinophilic Leukemia Peliosis Hepatis Periodontitis Pfeiffer Syndrome Plasmacytoma Plasminogen Deficiency, Type I Post-Transplant Lymphoproliferative Disease Prostate Cancer Prostatitis Pulmonary Embolism Pulmonary Fibrosis Pulmonary Fibrosis, Idiopathic Pulmonary Tuberculosis Pure Red-Cell Aplasia Purpura Purpura Fulminans Pyomyositis Rapp-Hodgkin Syndrome Refractory Anemia Retinitis Revesz Syndrome Rheumatoid Arthritis Riddle Syndrome Rothmund-Thomson Syndrome Sagittal Sinus Thrombosis Scalp-Ear-Nipple Syndrome Scott Syndrome Seckel Syndrome Severe Combined Immunodeficiency Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Shwachman-Diamond Syndrome Sinusitis Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity Spondylocarpotarsal Synostosis Syndrome Spondylometaphyseal Dysplasia, Sedaghatian Type Subcorneal Pustular Dermatosis Sveinsson Chorioretinal Atrophy Systemic Lupus Erythematosus Systemic Mastocytosis Three M Syndrome 1 Thrombocytopenia Thrombosis Thymic Dysplasia Thymoma Thyroiditis Toxoplasmoză Transient Erythroblastopenia of Childhood Transverse Myelitis Trisomy 1q Turner Syndrome Vasculitis Viral Hepatitis Vitamin B12 Deficiency Zygomycosis