Informaţii despre

Nume Porphyria Cutanea Tarda
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Other porphyria; Porphyria cutanea tarda
Clasificare anatomică Malacards Boli ale ochiului; Boli de piele; Boli hepatice; Boli nefrologice (ale rinichilor)
Boli din aceeaşi familie Familial Porphyria Cutanea Tarda; Porphyria Cutanea Tarda, Type I

Vezi şi

Boli A-Z Acquired Immunodeficiency Syndrome Acute Liver Failure Acute Non Lymphoblastic Leukemia Acute Porphyria Aging Alcohol Abuse Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Anemia, Sideroblastic, 1 Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Atransferrinemia Beta-Thalassemia Blood Group--Ahonen Blood Group, I System Breast Cancer Bullous Pemphigoid Calcinosis Cholangiocarcinoma Cholestasis Chorioretinitis Chronic Myelomonocytic Leukemia Chronic Venous Insufficiency Cicatricial Ectropion Cicatricial Pemphigoid Congenital Extrahepatic Portosystemic Shunt Conjunctival Squamous Cell Carcinoma Conjunctivitis Constrictive Pericarditis Coproporphyria, Hereditary Crest Syndrome Cutaneous Lupus Erythematosus Cutaneous Porphyria Dermatitis Dermatomyositis Diabetes Mellitus Discoid Lupus Erythematosus Ectropion Empty Sella Syndrome Eosinophilic Fasciitis Epidermolysis Bullosa Epidermolysis Bullosa Acquisita Epilepsy Erythema Elevatum Diutinum Familial Porphyria Cutanea Tarda Fanconi Anemia, Complementation Group E Fasciitis Folic Acid Deficiency Anemia Glomerulonephritis Granuloma Annulare Hairy Cell Leukemia Hansen's Disease Hemihyperplasia, Isolated Hemochromatosis, Type 1 Hemochromatosis Type 2 Hemoglobinopathy Hemolytic Anemia Hemosiderosis Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Hfe-Associated Hereditary Hemochromatosis Human Coronavirus Sensitivity Hyperferritinemia with or Without Cataract Hyperglycemia Hypertrichosis Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypopituitarism Ichthyosis, Congenital, Autosomal Recessive 11 Immune Suppression Inherited Metabolic Disorder Iron Metabolism Disease Iron Overload in Africa Lepromatous Leprosy Leukemia Lichen Planus Lipoid Proteinosis of Urbach and Wiethe Liver Cirrhosis Liver Disease Lupus Erythematosus Lymphoblastic Leukemia Lymphoid Leukemia Lymphoma Melioidosis Membranoproliferative Glomerulonephritis Metal Metabolism Disorder Multiple Sclerosis Mycobacterium Kansasii Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Nonalcoholic Steatohepatitis Ocular Cicatricial Pemphigoid Pancreatitis Pancreatitis, Hereditary Pdgfrb-Associated Chronic Eosinophilic Leukemia Pericarditis Peritonitis Porphyria Porphyria, Acute Intermittent Porphyria, Congenital Erythropoietic Porphyria Cutanea Tarda, Type I Porphyria Variegata Premature Ovarian Failure 7 Primary Syphilis Protoporphyria, Erythropoietic Refractory Anemia Renal Glucosuria Retinitis Pigmentosa and Erythrocytic Microcytosis Rheumatoid Arthritis Rhizomelic Chondrodysplasia Punctata, Type 2 Scleritis Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Siderosis Skin Disease Solar Urticaria Squamous Cell Carcinoma Subacute Cutaneous Lupus Erythematosus Syphilis Systemic Lupus Erythematosus Systemic Scleroderma Thalassemia Urticaria Vaginitis Venous Insufficiency Viral Hepatitis Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6