Informaţii despre

Nume Hemochromatosis, Type 1
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Disorders of iron metabolism
Clasificare anatomică Malacards Boli hepatice
Boli din aceeaşi familie Hemochromatosis Type 2; Hemochromatosis, Type 2a; Hemochromatosis, Type 2b; Hemochromatosis, Type 3; Hemochromatosis, Type 4; Hemochromatosis, Type 5

Vezi şi

Boli A-Z Aceruloplasminemia Adie Pupil Aging Alopecia Alopecia Areata Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-1-Antitrypsin Deficiency Alpha-Thalassemia Al-Raqad Syndrome Ancylostomiasis Androgen Insensitivity Syndrome, Mild Anemia, Sideroblastic, 1 Anemia, Sideroblastic, and Spinocerebellar Ataxia Aniridia 1 Anorexia Nervosa 1 Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Atransferrinemia Beta-Thalassemia Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock 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 Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Cardiac Arrhythmia Cataract Charge Syndrome Childhood Leukemia Chronic Pyelonephritis Cirrhosis, Familial Cleft Palate, Isolated Colitis Congenital Dyserythropoietic Anemia Congenital Hemolytic Anemia Crouzon Syndrome with Acanthosis Nigricans Deficiency Anemia Dermatitis Dermatophytosis Diabetes Mellitus Dilated Cardiomyopathy Duodenitis Dyskeratosis Congenita, X-Linked Endotheliitis Epileptic Encephalopathy, Early Infantile, 36 Extrinsic Allergic Alveolitis Familial Porphyria Cutanea Tarda Fanconi Anemia, Complementation Group E Fatty Liver Disease Feingold Syndrome 1 Friedreich Ataxia 1 Frontotemporal Dementia, Chromosome 3-Linked Fructose Intolerance, Hereditary Gilbert Syndrome Hajdu-Cheney Syndrome Headache Heme Oxygenase 1 Deficiency Hemochromatosis, Neonatal Hemochromatosis Type 2 Hemochromatosis, Type 2a Hemochromatosis, Type 2b Hemochromatosis, Type 3 Hemochromatosis, Type 4 Hemochromatosis, Type 5 Hemoglobinemia Hemoglobin H Disease Hemoglobinopathy Hemoglobinuria Hemosiderosis Hepatic Adenomas, Familial Hepatitis Hepatitis B Hepatitis C Hepatocellular Carcinoma Hereditary Spherocytosis Hfe-Associated Hereditary Hemochromatosis Hyperferritinemia with or Without Cataract Hyper Ige Syndrome Hyperinsulinemic Hypoglycemia, Familial, 6 Hyperuricemia Hypochromic Microcytic Anemia Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypotonia-Cystinuria Syndrome Hypotrichosis 1 Immunodeficiency 43 Inherited Metabolic Disorder Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies Iron Deficiency Anemia Iron Metabolism Disease Iron Overload in Africa Iron-Refractory Iron Deficiency Anemia Juvenile Hereditary Hemochromatosis Leukemia Liver Cirrhosis Liver Disease Long Qt Syndrome Lymphoblastic Leukemia Lymphoma Malignant Spiradenoma Meckel Syndrome, Type 1 Metal Metabolism Disorder Microcytic Anemia Migraine with or Without Aura 1 Mineral Metabolism Disease Mitochondrial Dna Depletion Syndrome 4a Multiple System Atrophy 1 Nutmeg Liver Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Pancreatitis, Hereditary Paroxysmal Nocturnal Hemoglobinuria Plague Polycystic Ovary Syndrome Polycythemia Polycythemia Vera Porphyria Porphyria Cutanea Tarda Porphyria Cutanea Tarda, Type I Porphyria Variegata Retinitis Retinitis Pigmentosa 7 Rhizomelic Chondrodysplasia Punctata, Type 2 Ring Chromosome 2 Sickle Cell Disease Sideroblastic Anemia Siderosis Superficial Siderosis Swayback Synovitis Testicular Yolk Sac Tumor Tetraamelia Syndrome, Autosomal Recessive Tfr2-Related Hereditary Hemochromatosis Thalassemia Tumoral Calcinosis, Hyperphosphatemic, Familial Ulcerative Colitis Undifferentiated Pleomorphic Sarcoma Wilson Disease Woodhouse-Sakati Syndrome