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Nume Porphyria
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice; Boli rare
Clasificare anatomică Malacards Boli de sânge
Boli din aceeaşi familie Acute Porphyria

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Boli A-Z Acquired Immunodeficiency Syndrome Actinic Prurigo Acute Interstitial Pneumonia Acute Leukemia of Ambiguous Lineage Acute Liver Failure Acute Myocardial Infarction Acute Non Lymphoblastic Leukemia Acute Pancreatitis Acute Porphyria Aging Agoraphobia Alacrima, Achalasia, and Mental Retardation Syndrome 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 Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Aminolevulinate Dehydratase Deficiency Porphyria Aminolevulinic Acid Dehydratase Deficiency Porphyria Amyloidosis Androgen Insensitivity Syndrome, Mild Anemia, Sideroblastic, 1 Aneurysm Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Antipyrine Metabolism Argininemia Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia Neuropathy Spectrum Atransferrinemia Atrial Fibrillation Autism Autoimmune Hepatitis Autonomic Dysfunction Autonomic Neuropathy Autosomal Dominant Disease Axonal Neuropathy Beta-Thalassemia Bipolar Disorder Blood Group--Ahonen Blood Group, I System Blood Group, Langereis System Bone Mineral Density Quantitative Trait Locus 1 Breast Cancer Brucellosis Bullous Pemphigoid Calcinosis Celiac Disease 1 Cerebral Atherosclerosis Cerebritis Chester Porphyria Chiari Malformation Cholangiocarcinoma Cholecystitis Cholelithiasis Cholestasis Chorioretinitis Chronic Myelomonocytic Leukemia Chronic Venous Insufficiency Cicatricial Ectropion Cicatricial Pemphigoid Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Iic Congenital Extrahepatic Portosystemic Shunt Conjunctival Squamous Cell Carcinoma Conjunctivitis Constipation Constrictive Pericarditis Coproporphyria, Hereditary Cortical Blindness Crest Syndrome Cryptorchidism, Unilateral or Bilateral Cutaneous Lupus Erythematosus Cutaneous Porphyria Cytochrome P450 2d6 Variant Dental Abscess Dermatitis Dermatitis Herpetiformis Dermatomyositis Diabetes Mellitus Discoid Lupus Erythematosus Dwarfism Dysautonomia Ectropion Empty Sella Syndrome Encephalitis Encephalopathy End Stage Renal Failure Eosinophilic Fasciitis Epidermolysis Bullosa Epidermolysis Bullosa Acquisita Epilepsy Erythema Elevatum Diutinum Erythropoietic Uroporphyria Associated with Myeloid Malignancy Familial Porphyria Cutanea Tarda Fanconi Anemia, Complementation Group E Fasciitis Focal Epilepsy Glioma Glomerulonephritis Granuloma Annulare Hairy Cell Leukemia Hansen's Disease Hantavirus Pulmonary Syndrome Heart and Brain Malformation Syndrome Heavy Metal Poisoning Helix Syndrome Hematopoietic Stem Cell Transplantation Hemihyperplasia, Isolated Hemochromatosis, Type 1 Hemolytic Anemia Hemosiderosis Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Human Coronavirus Sensitivity Huntington Disease Hydatidiform Mole, Recurrent, 1 Hypercholesterolemia, Autosomal Dominant, 3 Hypercholesterolemia, Familial Hyperferritinemia with or Without Cataract Hyperglycemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypertrichosis Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypocalcemia, Autosomal Dominant 1 Hypoganglionosis Hypopituitarism Ichthyosis, Congenital, Autosomal Recessive 11 Immunoglobulin Alpha Deficiency Inappropriate Adh Syndrome Inflammatory Bowel Disease Inherited Metabolic Disorder Intestinal Perforation Intracranial Aneurysm Intussusception 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 Macular Dystrophy, Retinal, 1, North Carolina Type Malaria Malignant Hypertension Melanoma Melioidosis Membranoproliferative Glomerulonephritis Meningitis Miller-Dieker Lissencephaly Syndrome Multiple Chemical Sensitivity Multiple Sclerosis Muscular Atrophy Mycobacterium Kansasii Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myocardial Infarction Myocarditis Nephrosclerosis Nephrotic Syndrome Neuritis Neurogenic Hypertension Neuropathy Nonalcoholic Steatohepatitis Ocular Cicatricial Pemphigoid Optic Neuritis Osteonecrosis Pancreatitis Pancreatitis, Hereditary Panic Disorder Pdgfrb-Associated Chronic Eosinophilic Leukemia Pericarditis Peritonitis Pfeiffer Syndrome Phaeochromocytoma Polycythemia Polymorphic Reticulosis Polyneuropathy Porphyria, Acute Hepatic Porphyria, Acute Intermittent Porphyria, Congenital Erythropoietic Porphyria Cutanea Tarda Porphyria Cutanea Tarda, Type I Porphyria Variegata Postural Hypotension Premature Ovarian Failure 7 Prieto X-Linked Mental Retardation Syndrome Primary Syphilis Progressive Muscular Atrophy Protoporphyria, Erythropoietic Protoporphyria, Erythropoietic, X-Linked Pseudoxanthoma Elasticum Pyridoxine Deficiency Rapp-Hodgkin Syndrome Rasmussen Encephalitis Refractory Anemia Renal Glucosuria Retinitis Retinitis Pigmentosa and Erythrocytic Microcytosis Rheumatoid Arthritis Rhizomelic Chondrodysplasia Punctata, Type 2 Schizoaffective Disorder Schizophrenia Scleritis Scleromalacia Perforans Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sideroblastic Anemia Siderosis Skin Disease Solar Urticaria Splenomegaly Spondylitis Spondyloarthropathy 1 Squamous Cell Carcinoma Status Epilepticus Subacute Cutaneous Lupus Erythematosus Sveinsson Chorioretinal Atrophy Syndrome of Inappropriate Antidiuretic Hormone Syphilis Systemic Lupus Erythematosus Systemic Scleroderma Tetraamelia Syndrome, Autosomal Recessive Thalassemia Three M Syndrome 1 Thrombocytopenia Thrombosis Thyroiditis Tularemia Typhoidal Tularemia Tyrosinemia Urticaria Vaginitis Venous Insufficiency Ventricular Septal Defect Viral Hepatitis Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 X-Linked Protoporphyria Yusho Disease