341
|
|
|
NK2 homeobox 1 |
BCH, BHC, NK-2, NKX2.1, NKX2A, NMTC1, T/EBP, TEBP, TITF1, TTF-1, TTF1 |
Benign hereditary chorea, Brain-lung-thyroid syndrome, Chorea, Choreatic disease, Choreoathetosis, Differentiated thyroid carcinoma, Hereditary ataxia, Interstitial lung disease, Lung disease, Neurodevelopmental disorder, Nonmedullary thyroid cancer, Papillary thyroid cancer |
342
|
|
|
NK2 homeobox 2 |
NKX2.2, NKX2B |
|
343
|
|
|
NK2 homeobox 3 |
CSX3, NK2.3, NKX2.3, NKX2C, NKX4-3 |
Ankylosing spondylitis, Autoimmune disease, Autoimmune thyroid disease, Celiac disease, Ulcerative colitis, Colorectal adenoma, Colorectal cancer, Common variable immunodeficiency, Crohn disease, Diverticular disease, Glomerulonephritis, Hypothyroidism, Inflammatory bowel disease, Juvenile idiopathic arthritis, Major depressive disorder, Psoriasis, Rheumatoid arthritis, Systemic lupus erythematosus, Diabetes mellitus type 1View all (4 more) |
344
|
|
|
NK2 homeobox 5 |
CHNG5, CSX, CSX1, HLHS2, NKX2.5, NKX2E, NKX4-1, VSD3 |
Aortic valve disease, Congenital hypothyroidism, Atrial fibrillation, Atrial flutter, Atrial septal defect, Atrioventricular block, Cardioembolic stroke, Cardiomegaly, Dilated cardiomyopathy, Cerebrovascular disorder, Thyroid agenesis, Congenital thyroid atrophy, Congenital heart disease, Congenital hypothyroidism due to absence of thyroid gland, Congenital hypothyroidism without goiter, Congenital septal defect of heart, Conotruncal cardiac defect, Deletion 5q35 syndrome, Double outlet right ventricle, Bicuspid aortic valve, Congenital asplenia, Congenital heart septal defect, Hereditary atrial fibrillation, Hereditary bundle branch system defect, Hypertrophic cardiomyopathy, Hypoplastic left heart syndrome, Interrupted aortic arch, Long qt syndrome, Myocardial infarction, Myotonic dystrophy, Splenic hypoplasia, Stroke, Tetralogy of fallot, Ventricular fibrillation, Ventricular septal defectView all (20 more) |
345
|
|
|
NK2 homeobox 6 |
CSX2, CTHM, NKX2F, NKX4-2 |
Alzheimer disease, Atrial fibrillation, Breast cancer, Cerebral palsy, Colorectal cancer, Congenital heart disease, Conotruncal cardiac defect, Gout, Hereditary atrial fibrillation, Metabolic syndrome, Prostate cancer, Tetralogy of fallot, Diabetes mellitus type 2, Vascular dementia, Ventricular septal defect |
346
|
|
|
NK3 homeobox 1 |
BAPX2, NKX3, NKX3.1, NKX3A |
|
347
|
|
|
NK3 homeobox 2 |
BAPX1, NKX3.2, NKX3B, SMMD |
|
348
|
|
|
NK6 homeobox 1 |
NKX6.1, NKX6A |
|
349
|
|
|
NK6 homeobox 2 |
GTX, NKX6.2, NKX6B, SPAX8 |
|
350
|
|
|
NK6 homeobox 3 |
NKX6.3 |
|
