Informaţii despre

Nume Methylmalonic Aciduria, Cblb Type
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Other disorders of branched-chain amino-acid metabolism
Clasificare anatomică Malacards Boli nefrologice (ale rinichilor)

Vezi şi

Boli A-Z 3-Methylcrotonyl-Coa Carboxylase Deficiency Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amblyopia Amino Acid Metabolic Disorder Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia Neuropathy Spectrum Biotin Deficiency Blood Group--Ahonen Blood Group, I System Cleft Larynx, Posterior Crouzon Syndrome with Acanthosis Nigricans Diabetes Mellitus Dystonia Ecthyma Encephalopathy End Stage Renal Failure Epilepsy Gout Growth Hormone Deficiency Hemolytic-Uremic Syndrome Hepatitis Holocarboxylase Synthetase Deficiency Homocysteinemia Homocystinuria Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Hyperglycemia Hyperlysinemia, Type I Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypotonia Ichthyosis Ichthyosis Vulgaris Isolated Methylmalonic Acidemia Isovaleric Acidemia Lung Disease Megaloblastic Anemia Metabolic Acidosis Methylmalonic Acidemia Cb1b Type Methylmalonic Acidemia with Homocystinuria Methylmalonic Aciduria and Homocystinuria, Cblc Type Methylmalonic Aciduria and Homocystinuria, Cbld Type Methylmalonic Aciduria and Homocystinuria, Cblf Type Methylmalonic Aciduria and Homocystinuria Type Cble Methylmalonic Aciduria and Homocystinuria Type Cblg Methylmalonic Aciduria, Cbla Type Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency Monocarboxylate Transporter 1 Deficiency Monoclonal Mast Cell Activation Syndrome Multiple Carboxylase Deficiency Myelomeningocele Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neuronitis Neuropathy Neutropenia Nondisjunction Ocular Motor Apraxia Organic Acidemia Pancreatitis Pancytopenia Peritonitis Propionic Acidemia Ptosis Pulmonary Hypertension Renal Tubular Acidosis Reye Syndrome Short Bowel Syndrome Succinate-Coa Ligase Deficiency Transcobalamin Ii Deficiency Vitamin B12 Deficiency Vitamin B12-Responsive Methylmalonic Acidemia Vitamin Metabolic Disorder