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Nume Vitamin B12 Deficiency
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice

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Boli A-Z Ablepharon-Macrostomia Syndrome Acquired Immunodeficiency Syndrome Acute Myocardial Infarction Adenocarcinoma Agammaglobulinemia Aging Alcohol Abuse Al-Raqad Syndrome Analbuminemia Aniridia 1 Anorexia Nervosa 1 Aphthous Stomatitis Aplastic Anemia Ariboflavinosis Arteries, Anomalies of Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Atrophic Gastritis Atrophic Glossitis Autonomic Dysfunction Autonomic Neuropathy Beta-Thalassemia Blepharospasm Blood Group--Ahonen Blood Group, Dombrock System 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 Breast Cancer Burning Mouth Syndrome Burns Cerebritis Cerebrovascular Disease Cervicitis Charles Bonnet Syndrome Chiari Malformation Childhood Disintegrative Disease Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Dementia Demyelinating Disease Diabetes Mellitus Diarrhea Duane Retraction Syndrome 1 Dystonia Endotheliitis End Stage Renal Failure Epidemic Typhus Focal Dystonia Folic Acid Deficiency Anemia Foster-Kennedy Syndrome Frontotemporal Dementia Galactosemia Gastric Adenocarcinoma Gastric Cancer Gastric Lymphoma Gastritis Glossitis Graves' Disease Helicobacter Pylori Infection Hemoglobin H Disease Hemoglobinopathy Hemolytic Anemia Hemosiderosis Hepatic Adenomas, Familial Hepatitis Hereditary Elliptocytosis Hereditary Spherocytosis Homocysteinemia Homocystinuria Homocystinuria Due to Cystathionine Beta-Synthase Deficiency Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Hyper Ige Syndrome Hyperphenylalaninemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Ileocolitis Immune System Disease Immunoglobulin Alpha Deficiency Inclusion Body Myositis Infertility Inflammatory Bowel Disease Iron Metabolism Disease Ischemia Johanson-Blizzard Syndrome Kagami-Ogata Syndrome Kaufman Oculocerebrofacial Syndrome Kwashiorkor Leukemia Lipoid Nephrosis Lymphoblastic Leukemia Lymphocytic Gastritis Lymphocytic Hypophysitis Lymphoma Malaria Marasmus Megaloblastic Anemia Methylmalonic Aciduria, Cblb Type Microcytic Anemia Monoclonal Mast Cell Activation Syndrome Mood Disorder Mouth Disease Mucositis Multiple Sclerosis Mungan Syndrome Myelomeningocele Myocardial Infarction Myoclonus Myositis Nervous System Disease Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neuroblastoma Neuropathy Nutritional Deficiency Disease Occipital Horn Syndrome Ophthalmia Neonatorum Overhydrated Hereditary Stomatocytosis Pancytopenia Periodontal Ehlers-Danlos Syndrome Pernicious Anemia Phenylketonuria Pneumonia Poems Syndrome Polyneuropathy Postural Orthostatic Tachycardia Syndrome Psychotic Disorder Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pure Red-Cell Aplasia Purpura Retinitis Scleritis Sensory Peripheral Neuropathy Short Bowel Syndrome Smooth Muscle Tumor Spasticity Spastic Paraparesis Spinal Cord Injury Spinal Stenosis Splenomegaly Stomatitis Subacute Delirium Thalassemia Thrombocytosis Thrombosis Thrombotic Thrombocytopenic Purpura Thyroiditis Transcobalamin Ii Deficiency Tremor Tropical Sprue Ventricular Fibrillation, Paroxysmal Familial, 1 Vitamin Metabolic Disorder West Syndrome Yellow Nail Syndrome