Informaţii despre

Nume Combined Immunodeficiency, X-Linked
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice
Clasificari ICD10 Combined immunodeficiency, unspecified
Clasificare anatomică Malacards Boli ale sistemului imunitar

Vezi şi

Boli A-Z Acquired Immunodeficiency Syndrome Acrodysostosis Actinic Keratosis Acute Graft Versus Host Disease Acute Leukemia Acute Lymphocytic Leukemia Adenocarcinoma Adenosine Deaminase Deficiency Adult Acute Lymphocytic Leukemia Adult T-Cell Leukemia Agammaglobulinemia Aging Alopecia Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha Chain Disease Alpha-Thalassemia Alport Syndrome, X-Linked Al-Raqad Syndrome Anaplastic Large Cell Lymphoma Aneurysm Angiostrongyliasis Aniridia 1 Anorexia Nervosa 1 Aplastic Anemia Artemis Deficiency Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Atrichia with Papular Lesions Attention Deficit-Hyperactivity Disorder Autoimmune Disease of Gastrointestinal Tract Autoimmune Lymphoproliferative Syndrome Autoimmune Lymphoproliferative Syndrome, Type V Autoimmune Myocarditis Autosomal Recessive Lymphoproliferative Disease Axillary Adenitis Bacterial Conjunctivitis Bare Lymphocyte Syndrome, Type I Bare Lymphocyte Syndrome, Type Ii B Cell Deficiency B-Cell Expansion with Nfkb and T-Cell Anergy B-Cell Lymphomas B Cell Prolymphocytic Leukemia Biotinidase Deficiency 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 Breast Cancer Brill-Zinsser Disease Brucellosis C1q Nephropathy Candidiasis Cartilage-Hair Hypoplasia Cataract 6, Multiple Types Cd40 Ligand Deficiency Central Nervous System Disease Central Nervous System Leukemia Cerebellar Degeneration Cerebellar Degeneration-Related Autoantigen 3 Cerebellar Hypoplasia Cerebral Lymphoma Cerebritis Cervicitis Chickenpox Childhood Leukemia Chlamydia Cholangitis Chondrodysplasia Punctata 2, X-Linked Dominant Chorioretinitis Chromosome 13q14 Deletion Syndrome Chronic Granulomatous Disease Chronic Interstitial Cystitis Chronic Mucocutaneous Candidiasis Cleft Lip/palate with Abnormal Thumbs and Microcephaly Coccidiosis Cohen-Gibson Syndrome Colitis Combined Cellular and Humoral Immune Defects with Granulomas Commensal Bacterial Infectious Disease Common Variable Immunodeficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Cytomegalovirus Congenital Hypogammaglobulinemia Congenital Subglottic Stenosis Congenital Syphilis Conjunctival Disease Cork-Handlers' Disease Coronin-1a Deficiency Cryofibrinogenemia Cryptococcosis Cutaneous T Cell Lymphoma Cystadenocarcinoma Cysticercosis Cytomegalovirus Infection Dacryoadenitis Demyelinating Disease Dermatitis Herpetiformis Dermatofibrosarcoma Protuberans Diabetes Insipidus Diabetes Mellitus Diffuse Cutaneous Mastocytosis Digeorge Syndrome Dilated Cardiomyopathy Down Syndrome Dysgammaglobulinemia Dyskeratosis Congenita Early Yaws Echinococcosis Encapsulated Thymoma Encephalitis Encephalitozoonosis Encephalopathy Endometriosis Endotheliitis Eosinophilic Meningitis Epidermodysplasia Verruciformis Erythema Elevatum Diutinum Exanthem Exanthema Subitum Extracutaneous Mastocytoma Exudative Glomerulonephritis Fanconi Anemia, Complementation Group E Fanconi Renotubular Syndrome 1 Fanconi Syndrome Fibrosarcoma Folate Malabsorption, Hereditary Follicular Lymphoma Gamma Heavy Chain Disease Gastric Cancer Gastroduodenitis Gastrointestinal Defects and Immunodeficiency Syndrome Giant Papillary Conjunctivitis Graft-Versus-Host Disease Granulomatous Hepatitis Graves' Disease Hairy Cell Leukemia Hansen's Disease Heavy Chain Disease Hematopoietic Stem Cell Transplantation Hemochromatosis, Type 2a Hemolytic Anemia Hemophagocytic Lymphohistiocytosis Hepatic Adenomas, Familial Hepatitis Hepatitis B Herpes Simplex Heterophyiasis Histiocytosis Human Immunodeficiency Virus Infectious Disease Human Immunodeficiency Virus Type 1 Hyperglobulinemic Purpura Hyperimmunoglobulin Syndrome Hyperlucent Lung Hypersensitivity Reaction Disease Hypersensitivity Reaction Type Iv Disease Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Immune Defect Due to Absence of Thymus Immune Deficiency Disease Immune System Disease Immunodeficiency 17 Immunodeficiency 18 Immunodeficiency 19 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 2 Immunodeficiency with Hyper-Igm, Type 1 Immunodeficiency with Hyper-Igm, Type 2 Immunodeficiency with Hyper-Igm, Type 3 Immunodeficiency with Hyper-Igm, Type 4 Immunoglobulin a Deficiency 1 Immunoglobulin E Concentration, Serum Immunoglobulin G Deficiency Inflammatory Bowel Disease Influenza Interleukin-7 Receptor Alpha Deficiency Intestinal Atresia Invasive Malignant Thymoma Jacobsen Syndrome Jak3-Deficient Severe Combined Immunodeficiency Juvenile Myelomonocytic Leukemia Keratoconjunctivitis Keratosis Kyphomelic Dysplasia Langerhans Cell Histiocytosis Leiomyomatosis Leukemia Leukocyte Disease Lichen Disease Lig4 Syndrome Light Fixation Seizure Syndrome Lipodystrophy, Partial, Acquired Lissencephaly 1 Listeriosis Liver Inflammatory Pseudotumor Lung Cancer Lung Disease Lung Lymphoma Lymphoblastic Leukemia Lymphokine Deficiency Lymphoma Lymphoma, Hodgkin, Classic Lymphoma, Non-Hodgkin, Familial Lymphopenia Lymphoproliferative Syndrome Malakoplakia Malaria Malignant Histiocytosis Mature B-Cell Neoplasm Megaloblastic Anemia Melanoma Meningitis Meningovascular Neurosyphilis Microcephaly Microscopic Colitis Microsporidiosis Miliary Tuberculosis Monoclonal Gammopathy of Uncertain Significance Monocytic Leukemia Monosomy 21 Mouth Disease Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Mumps Musical Perfect Pitch Myasthenia Gravis Mycobacterium Marinum Myelodysplastic Syndrome Myeloid Leukemia Myeloma, Multiple Myocarditis Natural Killer Cell Leukemia Nervous System Disease Neuroblastoma Neuronitis Neutropenia Noma Non-Secretory Myeloma Ocular Cicatricial Pemphigoid Ocular Melanoma Omenn Syndrome Opportunistic Mycosis Oral Squamous Cell Carcinoma Orbital Granuloma Osteochondroma Osteomyelitis Ovarian Cystadenocarcinoma Pancreatic Cancer Pancreatitis Pancytopenia Papillary Conjunctivitis Paralytic Poliomyelitis Paranasal Sinus Disease Paraneoplastic Cerebellar Degeneration Parasitic Helminthiasis Infectious Disease Parasitic Ichthyosporea Infectious Disease Parasitic Protozoa Infectious Disease Parotid Disease Pelvic Lipomatosis Plantar Wart Plasma Cell Neoplasm Plasmacytoma Plasma Protein Metabolism Disease Pneumonia Poliomyelitis Primary Agammaglobulinemia Primary Bacterial Infectious Disease Primary Effusion Lymphoma Progressive Multifocal Leukoencephalopathy Prolymphocytic Leukemia Prostate Cancer Prostatitis Protein-Losing Enteropathy Psoriasis Psoriasis 13 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hypertension Pulmonary Tuberculosis Purine Nucleoside Phosphorylase Deficiency Pyoderma Pyoderma Gangrenosum Recombinase Activating Gene 1 Deficiency Respiratory Syncytial Virus Infectious Disease Reticular Dysgenesis Retinitis Retinoblastoma Rheumatoid Arthritis Rhinosporidiosis Roifman-Chitayat Syndrome Rothmund-Thomson Syndrome Rubella Salivary Gland Disease Salpingo-Oophoritis Schistosomiasis Sclerosing Cholangitis Selective Igg Deficiency Disease Selective Immunoglobulin Deficiency Disease Severe Combined Immunodeficiency Severe Combined Immunodeficiency, Atypical Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Positive Severe Combined Immunodeficiency with Sensitivity to Ionizing Radiation Severe Combined Immunodeficiency, X-Linked Sezary's Disease Skeletal Dysplasias Small Intestine Lymphoma Spinocerebellar Ataxia, Autosomal Recessive 10 Squamous Cell Carcinoma Subacute Bacterial Endocarditis Subacute Thyroiditis T Cell Deficiency T-Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy T-Cell Leukemia Teratocarcinoma Tetanus Thalassemia Thrombocytopenia Thrombosis Thymic Dysplasia Thyroid Cancer Thyroiditis Tonsillitis Toxic Shock Syndrome Toxoplasmoză Transient Hypogammaglobulinemia of Infancy Trichostrongyloidiasis Tuberculoid Leprosy Tuberculous Empyema Urethritis Van Der Woude Syndrome 1 Ventilation Pneumonitis Vernal Conjunctivitis Virus Associated Hemophagocytic Syndrome Vulvovaginal Candidiasis Waldenstrom Macroglobulinemia West Syndrome Whim Syndrome Zap-70 Deficiency Zap70-Related Severe Combined Immunodeficiency