|
421
|
|
|
- |
- |
Cerebellar ataxia, Cleft palate and bilateral cleft lip, Congenital cardiomyopathy, Dementia, Developmental delay, Epilepsy, Hearing impairment, Leber hereditary optic neuropathy, Macular degeneration, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy with hearing impairment, Optic atrophy, Optic neuritis, Optic neuropathy, Parkinson disease, Peripheral neuropathy, Retinitis pigmentosa, Schizophrenia, Postaxial polydactyly, Venous thromboembolismView all (7 more) |
|
422
|
|
|
- |
- |
Cerebellar ataxia, Cleft palate and bilateral cleft lip, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy in association with hereditary ataxia, Parkinson disease, Retinitis pigmentosa, Postaxial polydactyly |
|
423
|
|
|
- |
- |
Alzheimer disease, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Developmental delay, Epilepsy, Leigh syndrome, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Myocardial infarction, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Parkinson disease, Retinitis pigmentosa, Postaxial polydactylyView all (1 more) |
|
424
|
|
|
- |
- |
Alzheimer disease, Attention deficit hyperactivity disorder, Bipolar disorder, Blepharoptosis, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Deafness, aminoglycoside-induced, Deafness, nonsyndromic sensorineural, mitochondrial, Deafness, sensorineural, autosomal-mitochondrial type, Bipolar depression, Developmental regression, Experimental diabetes, Diabetes mellitus type 2, Dysarthria, Global developmental delay, Leber hereditary optic neuropathy, Melas syndrome, Migraine, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Non-neoplastic peripheral nervous system disease, Obesity, Optic atrophy, Optic neuropathy, Parkinson disease, Hereditary parkinson disease, Peripheral neuropathy, Renal hypertension, Restrictive cardiomyopathy, Rheumatoid arthritis, Retinitis pigmentosa, Toxic shock syndrome, Postaxial polydactyly, Wolfram syndromeView all (20 more) |
|
425
|
|
|
NIMA related kinase 4 |
NRK2, STK2, pp12301 |
|
|
426
|
|
|
Nuclear receptor subfamily 2 group F member 1 |
BBOAS, BBSOAS, COUP-TFI, COUPTF1, EAR-3, EAR3, ERBAL3, SVP44, TCFCOUP1, TFCOUP1 |
|
|
427
|
|
|
Nuclear receptor subfamily 2 group F member 2 |
ARP-1, ARP1, CHTD4, COUPTF2, COUPTFB, COUPTFII, NF-E3, SRXX5, SVP40, TFCOUP2 |
|
|
428
|
|
|
NK2 homeobox 1 |
BCH, BHC, NK-2, NKX2.1, NKX2A, NMTC1, T/EBP, TEBP, TITF1, TTF-1, TTF1 |
|
|
429
|
|
|
Nuclear receptor subfamily 2 group E member 1 |
TLL, TLX, XTLL |
|
|
430
|
|
|
Nuclear receptor subfamily 2 group C member 1 |
TR2 |
|
