371
|
|
|
NADH:ubiquinone oxidoreductase subunit A9 pseudogene 1 |
dJ106I20.2 |
Curated: N/A
Unreviewed: N/A
|
372
|
|
|
NADH:ubiquinone oxidoreductase subunit AB1 |
ACP, ACP1, FASN2A, SDAP |
Curated: Alzheimer disease
Unreviewed: Adamantinous Craniopharyngioma, Adenocarcinoma, Anemia, Aniridia, Anxiety disorder, Arteriosclerosis, Asthma, Atherosclerosis, Autism, Autoimmune Diseases, Benign Neoplasm, Bipolar Disorder, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Cardiomyopathy, Cardiovascular disease, Cardiovascular Diseases, Colitis, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Congenital Cataract, Congenital Chromosomal Disease, Congestive Heart Failure, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Craniopharyngioma, Crohn Disease, Deficiency Of Glucose-6-Phosphate Dehydrogenase, Dementia, Diabetes, Diabetes Mellitus, Diabetic Retinopathy, Dyslipidemias, Endometrial carcinoma, Endometriosis, Epilepsy, Fanconi Anemia, Favism, Gastritis, Gastrointestinal neoplasm, Glioblastoma, Hairy Cell Leukemia, Hashimoto Disease, Heart Failure, Hemolysis, Hepatocellular carcinoma, Hepatolenticular Degeneration, Huntington disease, Immune system disease, Immune System Diseases, Inflammatory Bowel Disease, Intracranial Neoplasm, Ketosis, Lafora Disease, Leiomyoma, LEOPARD Syndrome, Leukemia, Liver carcinoma, Lung Cancer, Lung carcinoma, Lung neoplasms, Lupus Erythematosus, Lymphocytic Leukemia, Lymphoma, Machado-Joseph Disease, Malignant Neoplasm, Melanoma, Mental Depression, Mental Disorders, Metabolic Syndrome, Neoplasms, Neuroblastoma, Neurodegenerative disorder, Neurodegenerative Disorders, Noonan Syndrome, Obesity, Osteonecrosis, Osteoporosis, Parkinson disease, Prostatic neoplasm, Retinal Diseases, Rheumatoid arthritis, Schizophrenia, Seizure, Senile Dementia, Stomach Carcinoma, Stomach Neoplasms, Stroke, Thyroid Carcinoma, Tourette Syndrome, Trichohepatoenteric Syndrome, Ulcerative colitis, Uterine Fibroids, Varicocele
|
373
|
|
|
NADH:ubiquinone oxidoreductase subunit AB1 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
374
|
|
|
NADH:ubiquinone oxidoreductase complex assembly factor 1 |
CGI-65, CGI65, CIA30, MC1DN11 |
Curated: Mitochondrial complex deficiency, Mitochondrial disease
Unreviewed: Cardiomyopathy, Congestive Heart Failure, Developmental Delay, Diabetes Mellitus, Epileptic encephalopathy, Hearing Loss, Hypertrophic cardiomyopathy, Hypoglycemia, Isolated Complex I Deficiency, Leukodystrophy, Leukoencephalopathy, Microcephaly, Mitochondrial Complex Deficiency, Mitochondrial Diseases, Mitochondrial myopathy, Myopathy, Nystagmus, Osteoporosis, Ovarian neoplasm, Pancreatic neoplasm, Ptosis, Retinal Diseases, Scoliosis, Strabismus
|
375
|
|
|
NDUFAF1 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
376
|
|
|
NADH:ubiquinone oxidoreductase complex assembly factor 2 |
B17.2L, MC1DN10, MMTN, NDUFA12L, mimitin |
Curated: Alzheimer disease, Attention deficit hyperactivity disorder, Brain disease, Cannabis abuse, Cockayne syndrome, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Parkinson disease, Schizophrenia, Scoliosis, Substance abuse, Uv-sensitive syndrome
Unreviewed: Anemia, Apnea, Attention Deficit Hyperactivity Disorder, Carcinoma, Central Nervous System Inborn Metabolic Diseases, Cerebellar Ataxia, Developmental Delay, Diabetes Mellitus, Dysarthria, Dysphagia, Epileptic encephalopathy, Esophagus Neoplasm, Gastritis, Hearing Loss, HYPERTRICHOSIS, Hypertrophic cardiomyopathy, Hypoglycemia, Isolated Complex I Deficiency, Leigh Syndrome, Leigh Syndrome With Leukodystrophy, Leukodystrophy, Leukoencephalopathy, Mental retardation, Microcephaly, Mitochondrial Complex Deficiency, Mitochondrial Diseases, Mitochondrial myopathy, Mood swings, Multiple Congenital Anomalies, Nervous System Diseases, Neuroblastoma, Nystagmus, Optic Atrophy, Ovarian neoplasm, Ptosis, Respiratory Failure, Retinitis Pigmentosa, Retinoblastoma, Stomach neoplasms, Strabismus, Ventricular septal defect, Vitiligo
|
377
|
|
|
NDUFAF2 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
378
|
|
|
NDUFAF2 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
379
|
|
|
NADH:ubiquinone oxidoreductase complex assembly factor 3 |
2P1, C3orf60, E3-3, MC1DN18 |
Curated: Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease
Unreviewed: Anemia, Cardiomyopathy, Congestive Heart Failure, Developmental Delay, Developmental regression, Diabetes Mellitus, Dyskinetic Syndrome, Dysphagia, Epileptic encephalopathy, Hearing Loss, HYPERTRICHOSIS, Hypertrophic cardiomyopathy, Hypoglycemia, Isolated Complex I Deficiency, Leigh Syndrome, Leigh Syndrome With Cardiomyopathy, Leukodystrophy, Leukoencephalopathy, Mammary Neoplasms, Mental retardation, Microcephaly, Mitochondrial Complex Deficiency, Mitochondrial Diseases, Mitochondrial myopathy, Nervous System Diseases, Nystagmus, Optic Atrophy, Ptosis, Pulmonary Stenosis, Renal agenesis, Renal dysplasia, Respiratory Failure, Retinal Diseases, Strabismus
|
380
|
|
|
NADH:ubiquinone oxidoreductase complex assembly factor 4 |
C6orf66, HRPAP20, HSPC125, MC1DN15, My013, bA22L21.1 |
Curated: Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Prostate cancer, Stroke
Unreviewed: Breast Cancer, Breast Carcinoma, Breast neoplasm, Cardiomyopathy, Developmental Delay, Diabetes Mellitus, Epileptic encephalopathy, Hearing Loss, Hypertrophic cardiomyopathy, Hypoglycemia, Isolated Complex I Deficiency, Leigh Syndrome, Leukodystrophy, Leukoencephalopathy, Mammary Neoplasms, Microcephaly, Mitochondrial Complex Deficiency, Mitochondrial Diseases, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Myopathy, Nystagmus, Optic Atrophy, Ptosis, Spastic Quadriplegia, Strabismus
|