61
|
|
|
NAD(P)HX epimerase |
AIBP, APOA1BP, PEBEL, YJEFN1 |
Brain atrophy, Cerebellar edema, Cerebral atrophy, Developmental regression, Encephalopathy, Epileptic encephalopathy, Leukoencephalopathy, Encephalopathy with brain edema and/or leukoencephalopathy, Nystagmus, Respiratory failure, Skin erosion, Spinal cord diseases, Strabismus |
62
|
|
|
Sodium/potassium transporting ATPase interacting 4 |
C20orf58, FAM77A, bA261N11.2 |
|
63
|
|
|
NAD kinase 2, mitochondrial |
C5orf33, DECRD, MNADK, NADKD1 |
2,4-dienoyl-coa reductase deficiency, Central visual impairment, Cerebellar atrophy, Cerebral atrophy, Choreoathetosis, Developmental delay, Epileptic encephalopathy, Hyperlysinemia, Hypoplasia of corpus callosum, Leukodystrophy, Microcephaly, Hypotonia, Nystagmus, Pancreatitis, Progressive encephalopathy with leukodystrophy, Quadriplegia, Sleep apneaView all (2 more) |
64
|
|
|
Nuclear receptor coactivator 7 |
ERAP140, ESNA1, NCOA7-AS, Nbla00052, Nbla10993, TLDC4, dJ187J11.3 |
|
65
|
|
|
NOBOX oogenesis homeobox |
OG-2, OG2, OG2X, POF5, TCAG_12042 |
|
66
|
|
|
NADH:ubiquinone oxidoreductase complex assembly factor 6 |
C8orf38, FRTS5, MC1DN17, lncREST |
Alzheimer disease, Anemia, Cardiovascular diseases, Cerebellar ataxia, Developmental delay, Developmental regression, Diabetes mellitus, Dysarthria, Hypertrichosis, Hypertrophic cardiomyopathy, Mental retardation, Leigh syndrome, Leigh syndrome with leukodystrophy, Leukodystrophy, Lymphoblastic leukemia, Mitochondrial complex deficiency, Mood swings, Movement disorders, Nervous system diseases, Neuropathy, Nystagmus, Optic atrophy, Fanconi syndrome, Ptosis, Retinitis pigmentosa, Scoliosis, Strabismus, Ventricular septal defectView all (13 more) |
67
|
|
|
NK2 homeobox 6 |
CSX2, CTHM, NKX2F, NKX4-2 |
Aortic coarctation, Atrial fibrillation, Atrioventricular septal defect, Brachydactyly, Camptodactyly of fingers, Conotruncal heart defect, Cryptorchidism, Dolichocephaly, Double outlet right ventricle, Persistent truncus arteriosus, Polydactyly, Proptosis, Tetralogy of fallot, Transposition of great vessels |
68
|
|
|
NIMA related kinase 7 |
- |
|
69
|
|
|
Nucleolar protein 4 like |
C20orf112, C20orf113 |
|
70
|
|
|
Neurensin 1 |
VMP, p24 |
|