2941
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Metabolism of cobalamin associated A |
cblA |
Curated: Cataract, Deficiency anemia, Megaloblastic anemia, Methylmalonic acidemia, Vitamin b deficiency, Vitamin b12 deficiency, methylmalonic aciduria, cblA type
Unreviewed: Anemia, Colonic neoplasm, Cystic Fibrosis, Developmental Delay, Dimauro disease, Inborn Errors Of Metabolism, Intellectual developmental disorder, Ketonuria, Ketosis, Kidney failure, Metabolic syndrome, Methylmalonic aciduria, Neutropenia, Pancytopenia, Vitamin B12-Responsive Methylmalonic Acidemia
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2942
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Metabolism of cobalamin associated B |
ATR, CFAP23, cblB, cob |
Curated: Autoinflammatory syndrome, Cataract, Coronary artery disease, Major depressive disorder, Hyper-immunoglobulin d syndrome, Insomnia, Methylmalonic acidemia, Neurotic disorder, Polymyositis, Prostate cancer, Psychiatric disorders, Schizophrenia, methylmalonic aciduria, cblb type
Unreviewed: Alzheimer disease, Anemia, Anxiety Disorder, Aplastic anemia, Asthma, Atrophy, Autoimmune disease, Autoimmune Diseases, B-Cell Lymphoma, Breast disease, Breast neoplasm, Capillary infantile hemangioma, Carcinogenesis, Cardiomyopathy, Coronary Heart Disease, Deficiency Of Mevalonate Kinase, Developmental Delay, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Dyslipidemias, Gallbladder neoplasm, Gestational diabetes, Glioma, Graves Disease, Hereditary breast and ovarian cancer syndrome, Hypothyroidism, Interstitial nephritis, Intraductal noninfiltrating carcinoma, Intrahepatic Cholangiocarcinoma, Ischemic Stroke, Ketonuria, Ketosis, Leukemia, Lung carcinoma, Lung neoplasms, Lupus Erythematosus, Lymphatic metastasis, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphopenia, Lymphoproliferative Disorder, Malignant Neoplasm, Mental Depression, Methylmalonic aciduria, Multiple Sclerosis, Myeloid leukemia, Myeloproliferative disorder, Neoplasms, Neutropenia, Obesity, Pancytopenia, Polyglandular autoimmune syndrome, Sarcoidosis, Sezary syndrome, Squamous cell carcinoma, Stomach neoplasms, Systemic lupus erythematosus, Triple Negative Breast Neoplasms, Vitamin B12-Responsive Methylmalonic Acidemia, Waldenstrom macroglobulinemia
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2943
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Metabolism of cobalamin associated C |
cblC |
Curated: Hemolytic uremic syndrome, Cobalamin c disease, Intracellular cobalamin metabolism disorder, Methylmalonic acidemia, Retinitis pigmentosa
Unreviewed: Alzheimer disease, Anemia, Anorexia, Aortic dissection, Ataxia, Brain disease, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Cardiomyopathy, Cardiovascular disease, Cerebral cortical atrophy, Cobalamin deficiency, Cognition disorder, Cyanosis, Cystathioninemia, Delirium, Dementia, Developmental Delay, Developmental disability, Dysmorphic Features, Dysmorphism, Gamma-Cystathionase Deficiency, Glycogen Storage Disease, Headache, Heart failure, Hemolytic Uremic Syndrome, Homocystinuria, Hydrocephalus, Hyperhomocysteinemia, Hypersensitivity, Hypogonadism, Intellectual developmental disorder, Kidney Disease, Leukemia, Lung adenocarcinoma, Lung carcinoma, Macrotia, Macular degeneration, Macular dystrophy, Malignant Neoplasm, Megaloblastic anemia, Melanoma, Mental retardation, Metabolic syndrome, Methylmalonic Acidemia With Homocystinuria, Microcephaly, Movement Disorders, Myeloproliferative disorder, Neutropenia, Nystagmus, Paraplegia, Parkinson disease, Peripheral nervous system disease, Phenylketonuria, Psychotic disorders, Pulmonary arterial hypertension, Pulmonary hypertension, Renal cell carcinoma, Renal Insufficiency, Retinal Diseases, Retinitis Pigmentosa, Seizures, Thrombosis, Vitamin b deficiency
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2944
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MMACHC pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
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2945
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|
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Metabolism of cobalamin associated D |
C2orf25, CL25022, HMAD, MACD, MAHCD, cblD |
Curated: Lymphoblastic leukemia, Cobalamin c disease, Cobalamin metabolism disorder, Intracellular cobalamin metabolism disorder, Homocystinuria with megaloblastic anemia, Methylmalonic acidemia, inborn disorder of cobalamin metabolism and transport
Unreviewed: Anemia, Anorexia, Autonomic nervous system disease, Cerebral cortical atrophy, Cough, Developmental Delay, Hereditary sensory and autonomic neuropathy, Homocystinuria, Mental retardation, Methylcobalamin Deficiency, Methylmalonic acidemia with homocystinuria, Methylmalonic Aciduria, Nystagmus, Peripheral nervous system disease, Spastic Ataxia, Vitamin b deficiency
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2946
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|
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MMADHC divergent transcript |
- |
Curated: N/A
Unreviewed: Asthma, Bipolar Disorder, Bulimia
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2947
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|
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MMADHC pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
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2948
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|
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MMADHC pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
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2949
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|
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Monocyte to macrophage differentiation associated |
MMA, MMD1, PAQR11 |
Curated: Obesity, Schizophrenia
Unreviewed: Anemia, Arteriosclerosis, Arthritis, Atherosclerosis, Breast Cancer, Breast Carcinoma, Cobalamin deficiency, Colorectal neoplasm, Coronary artery disease, Crohn disease, Developmental Delay, Graves ophthalmopathy, Hyperhomocysteinemia, Hypertension, Impaired Cognition, Interstitial Nephritis, Ischemic Stroke, Kidney Disease, Limb-Girdle Muscular Dystrophy, Lung Cancer, Lung carcinoma, Malignant Neoplasm, Metabolic Diseases, Migraine, Moyamoya Disease, Muscular dystrophy, Myotonic dystrophy, Neoplasms, Neuropathy, Non-Alcoholic Fatty Liver Disease, Optic Neuropathy, Scleroderma, Scott Syndrome, Skin Lesion, Sleep Apnea, Urothelial Carcinoma, Vascular Diseases, Xeroderma Pigmentosum
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2950
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|
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Monocyte to macrophage differentiation associated 2 |
PAQR10 |
Curated: Alzheimer disease
Unreviewed: N/A
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