Informaţii despre

Nume Siderosis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Siderosis
Clasificare anatomică Malacards Boli ale ochiului; Boli respiratorii
Boli din aceeaşi familie Siderosis of Eye

Vezi şi

Boli A-Z Aceruloplasminemia Acute Pancreatitis Acute Porphyria Aging Alpha-1-Antitrypsin Deficiency Al-Raqad Syndrome Amyloidosis Amyloidosis, Hereditary, Transthyretin-Related Ancylostomiasis Anemia, Sideroblastic, 1 Aneurysm Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Anosmia Arteriovenous Fistula Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Asbestos Intoxication Asbestosis Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Atransferrinemia Aural Atresia, Congenital Back Pain Beta-Thalassemia Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen 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 Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brain Injury Cardiomyopathy, Familial Hypertrophic, 9 Cavernous Malformation Central Nervous System Origin Vertigo Cerebral Hemorrhage Cerebritis Cerebroretinal Microangiopathy with Calcifications and Cysts 1 Cervicitis Cholestasis Cold-Induced Sweating Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Ii Craniopharyngioma Cytomegalic Inclusion Disease Dementia Duodenitis Dyskeratosis Congenita, X-Linked Dyspepsia Dystonia Encephalopathy Endocarditis Endophthalmitis Endotheliitis Ependymoma Epilepsy Epileptic Encephalopathy, Early Infantile, 36 Familial Porphyria Cutanea Tarda Fatty Liver Disease Focal Dystonia Folic Acid Deficiency Anemia Galactosemia Germ Cells Tumors Headache Hemangioma Hemochromatosis, Neonatal Hemochromatosis, Type 1 Hemochromatosis Type 2 Hemoglobin H Disease Hemoglobinopathy Hemoglobinuria Hemosiderosis Hepatitis Hepatitis B Hepatitis C Hepatocellular Carcinoma Human Coronavirus Sensitivity Hydrocephalus Hyperferritinemia with or Without Cataract Hyperinsulinemic Hypoglycemia, Familial, 6 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypoascorbemia Hypochromic Microcytic Anemia Hypotrichosis 1 Infective Endocarditis Inherited Metabolic Disorder Intermediate Uveitis Interstitial Lung Disease Intracranial Aneurysm Intracranial Hypertension Intracranial Hypotension Intrahepatic Cholestasis Iron Metabolism Disease Iron Overload in Africa Lateral Sclerosis Leukemia Liver Cirrhosis Liver Disease Lung Cancer Lung Disease Lymphoblastic Leukemia Macular Dystrophy, Retinal, 1, North Carolina Type Meconium Ileus Melanoma Meningeal Melanocytoma Meningitis Meningocele Metal Metabolism Disorder Microcytic Anemia Motor Neuron Disease Mucositis Multiple Sclerosis Myxopapillary Ependymoma Nephrotic Syndrome Neurofibromatosis, Type I Neurofibromatosis, Type Iv, of Riccardi Neuronitis Neuropathy Pancreatitis Papillary Glioneuronal Tumors Paraganglioma Paroxysmal Nocturnal Hemoglobinuria Peritonitis Pilocytic Astrocytoma Pneumoconiosis Polyneuropathy Polyradiculopathy Porphyria Porphyria Cutanea Tarda Porphyria Cutanea Tarda, Type I Porphyria Variegata Pulmonary Fibrosis Refractory Anemia Renal Cell Carcinoma, Nonpapillary Retinitis Retinitis Pigmentosa 7 Rhizomelic Chondrodysplasia Punctata, Type 2 Ring Chromosome 2 Sensorineural Hearing Loss Sickle Cell Disease Silicosis Split-Hand/foot Malformation 1 Spontaneous Intracranial Hypotension Sudden Sensorineural Hearing Loss Superficial Siderosis Superficial Siderosis of the Central Nervous System Teratoma Thalassemia Thrombocytopenia Thrombosis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Traumatic Brain Injury Uveitis Viral Hepatitis