381
|
|
|
NADH:ubiquinone oxidoreductase complex assembly factor 4 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
382
|
|
|
NADH:ubiquinone oxidoreductase complex assembly factor 4 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
383
|
|
|
NADH:ubiquinone oxidoreductase complex assembly factor 4 pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
384
|
|
|
NADH:ubiquinone oxidoreductase complex assembly factor 4 pseudogene 4 |
- |
Curated: N/A
Unreviewed: N/A
|
385
|
|
|
NADH:ubiquinone oxidoreductase complex assembly factor 5 |
C20orf7, MC1DN16, bA526K24.2, dJ842G6.1 |
Curated: Leber hereditary optic neuropathy, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease
Unreviewed: Anemia, Cerebellar Ataxia, Choreoathetosis, Congenital abnormalities, Developmental Delay, Diabetes Mellitus, Dysarthria, Epileptic encephalopathy, Hearing Loss, Hydrops fetalis, Hypersensitivity, HYPERTRICHOSIS, Hypertrophic cardiomyopathy, Hypoglycemia, Infantile spasms, Isolated Complex I Deficiency, Leber Plus Disease, Leigh Syndrome, Leigh Syndrome With Leukodystrophy, Leukodystrophy, Leukoencephalopathy, Mental retardation, Microcephaly, Mitochondrial Complex Deficiency, Mitochondrial Diseases, Mitochondrial myopathy, Mood swings, Nervous System Diseases, Nystagmus, Optic Atrophy, Ptosis, Retinitis Pigmentosa, Strabismus, Ventricular septal defect
|
386
|
|
|
NADH:ubiquinone oxidoreductase complex assembly factor 6 |
C8orf38, FRTS5, MC1DN17, lncREST |
Curated: Alzheimer disease, Androgenetic alopecia, Cardiovascular disease, Coronary artery disease, De toni-debre-fanconi syndrome, Developmental regression, Diabetes mellitus, Fanconi renotubular syndrome, Gout, Hypertension, Keratoconus, Leigh syndrome, Metabolic syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Myocardial infarction, Nonalcoholic fatty liver disease, Peripheral neuropathy, Fanconi syndrome, Psoriasis, Diabetes mellitus type 2, Upper aerodigestive tract neoplasm, Vesicoureteral reflux
Unreviewed: Anemia, Breast neoplasm, Cardiovascular Diseases, Cerebellar Ataxia, Cerebral microangiopathy, Developmental Delay, Diabetes Mellitus, Dysarthria, Dystonia, Fanconi Anemia, Fanconi Syndrome, HYPERTRICHOSIS, Hypertrophic cardiomyopathy, Leigh Syndrome, Leigh Syndrome With Leukodystrophy, Leukodystrophy, Lymphoblastic Leukemia, Melas syndrome, Mental retardation, Mitochondrial Complex Deficiency, Mood swings, Movement Disorders, Nervous System Diseases, Neuropathy, Nystagmus, Optic Atrophy, Ptosis, Retinitis Pigmentosa, Scoliosis, Strabismus, Ventricular septal defect
|
387
|
|
|
NADH:ubiquinone oxidoreductase complex assembly factor 7 |
C2orf56, MidA, PRO1853 |
Curated: Alzheimer disease, Bipolar disorder, Lymphocytic leukemia, Gastroesophageal reflux disease, Inflammatory bowel disease, Ulcerative colitis
Unreviewed: N/A
|
388
|
|
|
NADH:ubiquinone oxidoreductase complex assembly factor 8 |
C17orf89, MC1DN34 |
Curated: Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease
Unreviewed: Frontotemporal dementia, Isolated Complex I Deficiency
|
389
|
|
|
NADH:ubiquinone oxidoreductase subunit B1 |
CI-MNLL, CI-SGDH, MNLL |
Curated: N/A
Unreviewed: N/A
|
390
|
|
|
NADH:ubiquinone oxidoreductase subunit B10 |
MC1DN35, PDSW |
Curated: Mitochondrial complex deficiency, Mitochondrial disease
Unreviewed: Cardiomyopathy, Developmental Delay, Diabetes Mellitus, Epileptic encephalopathy, Hearing Loss, Hypertrophic cardiomyopathy, Hypoglycemia, Isolated Complex I Deficiency, Leukodystrophy, Leukoencephalopathy, Microcephaly, Mitochondrial Complex Deficiency, Mitochondrial myopathy, Nystagmus, Ptosis, Strabismus
|