751
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NK2 homeobox 5 |
CHNG5, CSX, CSX1, HLHS2, NKX2.5, NKX2E, NKX4-1, VSD3 |
Curated: 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 defect, NKX2.5-related congenital, conduction and myopathic heart disease
Unreviewed: Aneurysm Of Aortic Arch, Aortic Coarctation, Aortic valve calcification, Aortic Valve Disease, Aortic Valve Insufficiency, Aortic Valve Sclerosis, Arteriosclerosis, Asplenia, Atherosclerosis, Atrial Fibrillation, Atrial Septal Defect, Atrial septal defect with atrioventricular conduction defects, Atrioventricular septal defect, Autism Spectrum Disorder, Brachydactyly, Bundle Branch Block, Camptodactyly of fingers, Cardiac Defects, Cardiomyopathy, Cardiovascular Diseases, Choroid Plexus Carcinoma, Ciliopathies, Complete Atrioventricular Block, Conduction Disorder Of The Heart, Congenital anomaly of limb, Congenital Exomphalos, Congenital heart defects, Congenital Heart Disease, Congenital hypertrophic pyloric stenosis, Congenital Hypothyroidism, Congenital hypothyroidism, nongoitrous, Congenital Myotonic Dystrophy, Congestive Heart Failure, Conotruncal heart defect, Coronary Heart Disease, Cryptorchidism, Deletion 5q36, Developmental Delay, Dolichocephaly, Double Outlet Right Ventricle, Down Syndrome, Dwarfism, Ebstein anomaly of the tricuspid valve, Gastrointestinal stromal tumor, Heart Block, Heart Diseases, Heart Septal Defects, Hereditary Bundle Branch System Defect, Holt-Oram Syndrome, Hypersomnia, Hypertension, Hypoplastic aortic arch, Hypoplastic Left Heart Syndrome, Hypothyroidism, Ischemic Stroke, Leiomyosarcoma, Lymphoblastic Leukemia, Lymphoproliferative Disorder, Macroglossia, Mental retardation, Mitral Valve Stenosis, Monosomy 5q35, Muscular ventricular septal defect, Myocardial Infarction, Neoplasms, Noncompaction cardiomyopathy, Paroxysmal atrial fibrillation, Patent ductus arteriosus, Patent foramen ovale, Persistent truncus arteriosus, Peutz-Jeghers Syndrome, Polydactyly, Progressive Cardiac Conduction Defect, Proptosis, Prostate cancer, Scleroderma, Secundum atrial septal defect, Splenic Hypoplasia, Tetralogy of Fallot, Thyroid Agenesis, Thyroid Dysgenesis, Thyroid Hypoplasia, Transposition Of Great Vessels, Ventricular arrhythmia
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752
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NK2 homeobox 6 |
CSX2, CTHM, NKX2F, NKX4-2 |
Curated: 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
Unreviewed: Aortic Coarctation, Aplasia of the thymus, Atrial Fibrillation, Atrioventricular septal defect, Brachydactyly, Camptodactyly of fingers, Conotruncal heart defect, Coronary Heart Disease, Cryptorchidism, DiGeorge Syndrome, Dolichocephaly, Double Outlet Right Ventricle, Persistent truncus arteriosus, Polydactyly, Proptosis, Shprintzen-Goldberg Syndrome, Tetralogy of Fallot, Transposition Of Great Vessels
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753
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NK2 homeobox 8 |
NKX2.8, NKX2H, Nkx2-9 |
Curated: N/A
Unreviewed: Esophageal Carcinoma, Esophagus Neoplasm, Lung Cancer, Lung carcinoma, Malignant Neoplasm, Neoplasms, Neural Tube Defect, Ovarian cancer, Ovarian Epithelial carcinoma, Spina Bifida
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754
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NK3 homeobox 1 |
BAPX2, NKX3, NKX3.1, NKX3A |
Curated: Oligodendroglioma, Prostate cancer, Prostatic neoplasms
Unreviewed: Breast Cancer, Breast Carcinoma, Carcinoma, Liver carcinoma, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoid leukemia, Metastatic Prostate Carcinoma, Neoplasm, Neoplasms, Prostatic Neoplasms
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755
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NK3 homeobox 2 |
BAPX1, NKX3.2, NKX3B, SMMD |
Curated: Connective tissue disease, Desbuquois syndrome
Unreviewed: Lymphoblastic Leukemia, Macrocephaly, Malignant Neoplasm, Microtia, Osteochondrodysplasia, Pyle Metaphyseal Dysplasia, Skeletal Dysplasia, Spondylo-Megaepiphyseal-Metaphyseal Dysplasia, Stomach Carcinoma, Stomach Neoplasms
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756
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NK6 homeobox 1 |
NKX6.1, NKX6A |
Curated: Diabetes mellitus type 2, Melanoma, Scoliosis
Unreviewed: Cervical Cancer, Cervical Intraepithelial Neoplasia, Cervical Tumor, Cervix carcinoma, Diabetes Mellitus, Mason type diabetes, Nephroblastoma
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757
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NK6 homeobox 2 |
GTX, NKX6.2, NKX6B, SPAX8 |
Curated: Spastic ataxia
Unreviewed: Bladder carcinoma, Bladder Neoplasm, Brain Neoplasms, Cerebellar atrophy, Cerebral Atrophy, Developmental Delay, Dysarthria, Epilepsy, Hypomyelinating Leukodystrophy, Hypoplasia Of Corpus Callosum, Hypotonia, Impaired Cognition, Kidney Disease, Leukodystrophy, Mental retardation, Motor delay, Neoplasms, Nystagmus, Oligodendroglioma, Pancreatic adenocarcinoma, Scoliosis, Spastic Ataxia, Spastic Ataxia, with hypomylineating leukodystrophy, Strabismus, Urinary bladder cancer
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758
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NK6 homeobox 3 |
NKX6.3 |
Curated: Diabetes mellitus, Diabetic eye disease, Diabetic neuropathy, Insomnia, Diabetes mellitus type 2
Unreviewed: Diffuse Lymphoma, Lymphoma
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759
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Notchless homolog 1 |
HUSSY7, NLE, Rsa4 |
Curated: N/A
Unreviewed: Attention deficit hyperactivity disorder, Breast Cancer, Hemolytic Uremic Syndrome, Vitiligo, Vitiligo-associated SYSTEMIC LUPUS ERYTHEMATOSUS
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760
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Neuroligin 1 |
NL1, NLG1 |
Curated: Asthma, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Insomnia, Irritable bowel syndrome, Major depressive disorder, Metabolic syndrome, Migraine, Osteoarthritis, Periodontitis, Willis-ekbom disease, Schizophrenia, Scoliosis, Substance abuse, Diabetes mellitus type 2
Unreviewed: Alzheimer disease, Amnesia, Amyloidosis, Attention Deficit Hyperactivity Disorder, Autism spectrum disorder, Bipolar Disorder, Cognition disorder, Colorectal neoplasm, Corticobasal degeneration, Diabetes Mellitus, Hirschsprung Disease, Hypertension, Leukemia, Mental retardation, Motion Sickness, Nervous System Disorder, Neurodegenerative disorder, Progressive supranuclear palsy, Prostatic neoplasm, Stress Disorder, Thrombophilia
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