8171
|
|
|
Mitochondrial fission regulator 1 |
CHPPR, FAM54A2 |
|
8172
|
|
|
Mitochondrial ribosome associated GTPase 1 |
GTP, GTPBP7 |
|
8173
|
|
|
Mitochondrial ribosome associated GTPase 2 |
GTPBP5, ObgH1, dJ1005F21.2 |
|
8174
|
|
|
Methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1 |
CIMAH, MTHFC, MTHFD |
Bipolar disorder, Cardiac valvular dysplasia, Cleft palate, Cleft lip, Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia, Combined immunodeficiency-megaloblastic anemia due to methylenetetrahydrofolate dehydrogenase 1 deficiency, Complete unilateral cleft lip, Down syndrome, Hypothyroidism, Major depressive disorder, Neural tube defect, Neural tube defects, x-linked, Neural tube defects, folate-sensitive, Ovarian cancer, Schizophrenia, Severe combined immunodeficiency, Tetralogy of fallotView all (2 more) |
8175
|
|
|
Methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1 like |
FTHFSDC1, MTC1THFS, dJ292B18.2 |
|
8176
|
|
|
Methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase |
NMDMC |
|
8177
|
|
|
Methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2 like |
- |
|
8178
|
|
|
Methylenetetrahydrofolate reductase |
- |
Alzheimer disease, Amyotrophic lateral sclerosis, Anemia, Sickle cell anemia, Anencephaly, Angle closure glaucoma, Ankylosing spondylitis, Rheumatoid arthritis, Asthma, Atherosclerosis, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Blood coagulation disorder, Brain ischemia, Breast neoplasms, Cardiovascular disease, Carotid artery stenosis, Ischemic stroke, Cerebrovascular disorder, Cervical dysplasia, Ischemic heart disease, Cleft lip, Clubfoot, Colonic neoplasms, Colorectal neoplasms, Complete unilateral cleft lip, Congenital clubfoot, Congenital heart defects, Coronary artery disease, Coronary restenosis, Crohn disease, Deficiency anemia, Vascular dementia, Bipolar depression, Major depressive disorder, Dermatologic disorder, Diabetes mellitus type 1, Diabetes mellitus type 2, Diabetic angiopathies, Diabetic peripheral angiopathy, Diabetic retinopathy, Digestive system disease, Discordant ventriculoarterial connection, Mitral valve disease, Eye disorder, Down syndrome, Endometrial neoplasms, Age-related macular degeneration, Fatty liver, Fatty liver, alcoholic, Gastrointestinal disease, Glaucoma, Global developmental delay, Glomerulonephritis, Graft-versus-host disease, Graves disease, Congenital heart defect, Hematologic disease, Hemophilia a, Hepatic vein thrombosis, Hepatic veno occlusive disease, Hyperhomocysteinemia, Hypersensitivity, Hypertension, Hypopituitarism, Female infertility, Male infertility, Inflammatory bowel disease, Kidney disease, Kidney failure, Lymphocytic b-cell leukemia, Liver cirrhosis, Liver disease, Lung neoplasms, Lymphoma, Malnutrition, Meniere disease, Microvascular angina, Migraine, Mood disorder, Moyamoya disease, Mucositis, Multiple sclerosis, Myocardial infarction, Myocardial ischemia, Necrosis, Nephrosclerosis, Nervous system disease, Neural tube defect, Neural tube defects, x-linked, Neural tube defects, folate-sensitive, Neutropenia, Nonalcoholic fatty liver disease, Orofacial cleft, Parkinson disease, Peripheral arterial disease, Portal vein thrombosis, Preeclampsia, Prostatic neoplasms, Rheumatic disease of mitral valve, Rheumatic mitral regurgitation, Schizophrenia, Skin disease, Stomach neoplasms, Stroke, Tetralogy of fallot, Thrombocytopenia, Thrombophilia, Transposition of the great arteries, Depression, Urinary bladder neoplasms, Uterine disease, Uterine neoplasms, Vascular disease, Venous thrombosisView all (102 more) |
8179
|
|
|
Methenyltetrahydrofolate synthetase |
HsT19268, NEDMEHM |
|
8180
|
|
|
Methenyltetrahydrofolate synthetase domain containing |
- |
|
