391
|
|
|
NADH:ubiquinone oxidoreductase subunit B10 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
392
|
|
|
NADH:ubiquinone oxidoreductase subunit B10 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
393
|
|
|
NADH:ubiquinone oxidoreductase subunit B11 |
CI-ESSS, ESSS, MC1DN30, NP17.3, Np15, P17.3 |
Curated: Microphthalmia, Mitochondrial complex deficiency, Mitochondrial disease, Neurodevelopmental disorder
Unreviewed: Absence Of Septum Pellucidum, Agenesis Of Corpus Callosum, Ambiguous Genitalia, Anemia, Aphasia, Atherosclerosis, Atresia Of Nasolacrimal Duct, Atrial Septal Defect, Cardiomyopathy, Cataract, Cockayne syndrome, Cognition disorder, Colpocephaly, Congenital Anomaly Of Rectum, Congenital Coloboma Of Iris, Congenital diaphragmatic hernia, Congestive Heart Failure, Developmental Delay, Developmental disability, Diabetes Mellitus, Dwarfism, Dysphasia, Epileptic encephalopathy, Epispadias, Glaucoma, Hearing Loss, Heart Septal Defects, Hereditary Leber Optic Atrophy, Histiocytoid Cardiomyopathy, Hydrocephalus, Hyperplasia, Hypertrophic cardiomyopathy, Hypertrophy Of Clitoris, Hypoglycemia, Hypospadias, Imperforate anus, Isolated Complex I Deficiency, Kidney disease, Leukodystrophy, Leukoencephalopathy, Linear Skin Defects With Multiple Congenital Anomalies, Liver disease, Male Pseudohermaphroditism, Mandibular aplasia, Memory disorders, Mental retardation, Microcephaly, Micrognathism, Microphthalmia With Linear Skin Defects Syndrome, Microphthalmos, Mitochondrial Complex Deficiency, Mitochondrial Diseases, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Mitral Valve Prolapse, Myopia, Necrosis, Neuroblastoma, Nystagmus, Overriding aorta, Ovotestis, Penis Agenesis, Posterior embryotoxon, Ptosis, Respiratory Failure, Retinal Dysplasia, Retinal Dystrophy, Retinitis Pigmentosa, Sclerocornea, Sideroblastic Anemia, Sideroblastic Anemia, X-Linked, Specific Learning Disorder, Status Epilepticus, Strabismus, Syndromic microphthalmia, Tricuspid Valve Insufficiency, Tricuspid Valve Prolapse, True Hermaphroditism, Venous thrombosis, Ventricular Fibrillation, Ventricular septal defect, Ventricular tachycardia, Vitritis
|
394
|
|
|
NADH:ubiquinone oxidoreductase subunit B11 pseudogene 1 |
NDUFB11P |
Curated: N/A
Unreviewed: N/A
|
395
|
|
|
NADH:ubiquinone oxidoreductase subunit B1 pseudogene 1 |
NDUFB1P, bcm3095 |
Curated: N/A
Unreviewed: N/A
|
396
|
|
|
NADH:ubiquinone oxidoreductase subunit B1 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
397
|
|
|
NADH:ubiquinone oxidoreductase subunit B2 |
AGGG, CI-AGGG |
Curated: Diabetes mellitus type 2
Unreviewed: Alzheimer disease, Behcet Syndrome, Carpal Tunnel Syndrome, Colorectal Cancer, Glioblastoma, Graves Disease, Hashimoto Disease, Liver carcinoma, Liver cirrhosis, Neoplasms, Precocious Pubarche, Prostate cancer, Sepsis, Thrombosis, Venous thromboembolism
|
398
|
|
|
NDUFB2 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
399
|
|
|
NADH:ubiquinone oxidoreductase subunit B2 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
400
|
|
|
NADH:ubiquinone oxidoreductase subunit B3 |
B12, CI-B12, MC1DN25 |
Curated: Congenital cataract, Developmental regression, Mitochondrial complex deficiency, Mitochondrial disease
Unreviewed: Alzheimer disease, Anemia, Autoimmune lymphoproliferative disorder, Benign mucous membrane pemphigoid, Breast Cancer, Breast Carcinoma, Cerebral microangiopathy, Developmental Delay, Diabetes Mellitus, Epileptic encephalopathy, Epithelial ovarian carcinoma, Fatty liver, alcoholic, Growth disorder, Hearing Loss, Homocystinuria, Hypersensitivity, Hypertrophic cardiomyopathy, Hypoglycemia, Isolated Complex I Deficiency, Leukodystrophy, Leukoencephalopathy, Melas syndrome, Methylmalonic acidemia, Microcephaly, Mitochondrial Complex Deficiency, Mitochondrial Diseases, Mitochondrial myopathy, Multiple Congenital Anomalies, Myopathy, Nystagmus, Ptosis, Selective immunoglobulin a deficiency, Strabismus, Vitiligo
|