Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity

Nume		Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity
Pagina Web		www.malacards.org
Clasificare globală Malacards		Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10		Disorders of sulfur-bearing amino-acid metabolism
Clasificare anatomică Malacards		Boli neuronale

Boli A-Z		Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Amino Acid Metabolic Disorder Angelman Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Blood Group--Ahonen Blood Group, I System Breast Reconstruction Cerebritis Cerebrovascular Disease Colorectal Adenoma Encephalopathy Fetal Akinesia Deformation Sequence Homocysteinemia Homocystinuria Megaloblastic Anemia Methylmalonic Aciduria, Cblb Type Microcephaly Mthfr Gene Variant Myelomeningocele Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neuropathy Paraplegia Pulmonary Embolism Spasticity Spondyloocular Syndrome Thoracic Outlet Syndrome Transcobalamin Ii Deficiency Vitamin B12 Deficiency Vitamin Metabolic Disorder