Dyskeratosis Congenita

Informaţii despre

Nume		Dyskeratosis Congenita
Pagina Web		www.malacards.org
Clasificare globală Malacards		Boli fetale; Boli genetice; Boli rare
Clasificari ICD10		Constitutional aplastic anaemia; Other specified congenital malformations of skin
Clasificare anatomică Malacards		Boli ale ochiului; Boli ale sistemului imunitar; Boli de piele; Boli de sânge; Boli neuronale
Boli din aceeaşi familie		Dyskeratosis Congenita Autosomal Dominant; Dyskeratosis Congenita Autosomal Recessive; Dyskeratosis Congenita, Autosomal Dominant 1; Dyskeratosis Congenita, Autosomal Dominant 2; Dyskeratosis Congenita, Autosomal Dominant 3; Dyskeratosis Congenita, Autosomal Dominant 6; Dyskeratosis Congenita, Autosomal Recessive 1; Dyskeratosis Congenita, Autosomal Recessive 2; Dyskeratosis Congenita, Autosomal Recessive 3; Dyskeratosis Congenita, Autosomal Recessive 5; Dyskeratosis Congenita, Autosomal Recessive 6

Vezi şi

Boli A-Z		46,xy Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy Acrofacial Dysostosis, Catania Type Acute Cholinergic Dysautonomia Adenocarcinoma Aging Albinism 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 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins Amenorrhea Anemia of Prematurity Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Aplastic Anemia Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Autoimmune Lymphoproliferative Syndrome, Type V Autoinflammation with Infantile Enterocolitis Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bowen's Disease Brain Small Vessel Disease with or Without Ocular Anomalies Bronchiolitis Bronchiolitis Obliterans Candidiasis Cataract Cerebellar Hypoplasia Chanarin-Dorfman Syndrome Choanal Atresia, Posterior Chondrodysplasia Punctata Syndrome Chronic Graft Versus Host Disease Coats Disease Cole Disease Colitis Common Variable Immunodeficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Iic Congenital Dyserythropoietic Anemia Congenital Hypothyroidism Congenital Intrauterine Infection-Like Syndrome Corneal Dystrophy, Avellino Type Cyanosis, Transient Neonatal Cytomegalovirus Retinitis Diabetes Mellitus Diffuse Mesangial Sclerosis Dubowitz Syndrome Dyskeratosis Congenita Autosomal Dominant Dyskeratosis Congenita, Autosomal Dominant 1 Dyskeratosis Congenita Autosomal Recessive Dyskeratosis Congenita, Autosomal Recessive 1 Dyskeratosis Congenita, X-Linked Dysphagia Ectodermal Dysplasia Emery-Dreifuss Muscular Dystrophy Enterocolitis Epidermodysplasia Verruciformis Exudative Vitreoretinopathy Fanconi Anemia, Complementation Group E Gastric Adenocarcinoma Gingivitis Graft-Versus-Host Disease Hematopoietic Stem Cell Transplantation Hemolytic Anemia Hepatitis Hepatopulmonary Syndrome Horseshoe Kidney Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypogonadism Ichthyosis Prematurity Syndrome Idiopathic Inflammatory Myopathy Incontinentia Pigmenti Inherited Bone Marrow Failure Syndromes Interstitial Lung Disease Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies Keratoacanthoma Kindler Syndrome Laryngitis Leukemia Leukoplakia Limbal Stem Cell Deficiency Lipoid Proteinosis of Urbach and Wiethe Liver Disease Lung Disease Lutheran Suppressor, X-Linked Lymphoblastic Leukemia Melanoma Microcephaly Multiple Mitochondrial Dysfunctions Syndrome 5 Muscular Dystrophy Myelodysplastic Syndrome Myopathy Nasopharyngitis Neurofibroma Neuropathy Neutropenia Ocular Albinism Oral Leukoplakia Oral Squamous Cell Carcinoma Pancytopenia Periodontal Disease Periodontitis Pharyngitis Pneumonia Poikiloderma with Neutropenia Portal Hypertension Pulmonary Arteriovenous Malformation Pulmonary Fibrosis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Fibrosis, Idiopathic Rapp-Hodgkin Syndrome Reticulohistiocytic Granuloma Retinal Telangiectasia Retinitis Revesz Syndrome Rothmund-Thomson Syndrome Schizophrenia Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Skin Disease Spondylocarpotarsal Synostosis Syndrome Squamous Cell Carcinoma Steatocystoma Multiplex Terminal Osseous Dysplasia Thrombocytopenia Thrombosis Tongue Cancer Torch Syndrome Urinary Tract Obstruction Wilson-Turner X-Linked Mental Retardation Syndrome