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291
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|
|
Notch receptor 2 |
AGS2, HJCYS, hN2 |
Acquired kyphoscoliosis, Acroosteolysis, Acrosteolysis, Alagille syndrome, Anaplastic astrocytoma, Aortic valve sclerosis, Arnold-chiari malformation, Arteriohepatic dysplasia, Astrocytoma, Atrial septal defect, B-cell lymphocytosis, Benign neoplasm of bladder, Urinary bladder cancer, Bladder neoplasm, Bladder carcinoma, Brachydactyly, Breast adenocarcinoma, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Cataract, Cerebral primitive neuroectodermal tumor, Uterine cervix neoplasm, Cervical cancer, Cholestatic liver disease, Congenital clubfoot, Congenital coloboma of iris, Dislocated radial head, Congenital epicanthus, Congenital exomphalos, Pulmonary hypoplasia, Congenital kyphoscoliosis, Congenital malrotation of intestine, Congenital pectus carinatum, Coronary heart disease, Cryptorchidism, Defect of skull ossification, Diabetes mellitus, Diffuse lymphoma, Digestive system neuroendocrine neoplasm, Dolichocephaly, Dwarfism, Ependymoblastoma, Esophagus neoplasm, Fibrillary astrocytoma, Gastric cancer, Gemistocytic astrocytoma, Giant cell glioblastoma, Glioblastoma, Grade i astrocytoma, Hajdu-cheney syndrome, Hearing loss, Heart septal defects, High palate, Hydrocephalus, Hypertension, Hypospadias, Intracranial astrocytoma, Leukemia, Lung neoplasms, Lung cancer, Lupus erythematosus, Lymphoma, Lymphoblastic leukemia, Macrocephaly, Marfan syndrome, Medulloepithelioma, Mesomelia, Micrognathism, Microstomia, Mitral valve stenosis, Multiple renal cysts, Myopia, Nervous system diseases, Neuroectodermal tumors, Oligoastrocytoma, Osteochondrodysplasia, Osteopenia, Osteoporosis, Patent ductus arteriosus, Periocular capillary hemangioma, Periodontitis, Peripheral pulmonary artery stenosis, Platybasia, Posterior embryotoxon, Protoplasmic astrocytoma, Pulmonary stenosis, Renal cyst, Renal hypoplasia, Renal insufficiency, Respiratory failure, Scoliosis, Skeletal dysplasia, Skin cancer, Skin neoplasms, Sleep apnea, Spongioblastoma, Stomach neoplasms, Synophrys, Syringomyelia, Tetralogy of fallot, Ventricular septal defectView all (88 more) |
|
292
|
|
|
Notch receptor 3 |
CADASIL, CADASIL1, CASIL, IMF2, LMNS |
Aphasia, Arachnoid cyst, Arnold-chiari malformation, Atherosclerosis, Benign neoplasm of nervous system, Breast cancer, Mammary neoplasms, Breast carcinoma, Cadasil syndrome, Carcinoma, Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy and migraine, Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy, Cerebral cortical atrophy, Cerebral ischemia, Chondrocalcinosis, Common migraine, Congenital coloboma of iris, Congenital epicanthus, Congenital exomphalos, Congenital meningocele, Congenital pectus excavatum, Cranial nerve paralysis, Cryptorchidism, Dementia, Developmental delay, Developmental regression, Dolichocephaly, Dwarfism, Epileptic encephalopathy, Esophagus neoplasm, Vascular leukoencephalopathy, Giant cell glioblastoma, Glioblastoma, Hearing loss, Hemiplegia/hemiparesis, High palate, Hypercalcemia, Hypertension, Hypoglycemia, Impaired cognition, Intestinal obstruction, Ischemic stroke, Lateral meningocele syndrome, Leukoencephalopathy, Liver carcinoma, Lung carcinoma, Lung neoplasms, Lung cancer, Marfan syndrome, Mental depression, Micrognathism, Migraine, Motor delay, Multicystic renal dysplasia, Myofibromatosis, Nonarteritic anterior ischemic optic neuropathy, Pancreatic neoplasm, Pancreatic ductal carcinoma, Patent ductus arteriosus, Platybasia, Posteriorly rotated ear, Proptosis, Pseudobulbar palsy, Ptosis, Scoliosis, Sensory neuropathy, Skin cancer, Skin neoplasms, Stroke, Subcortical dementia, Subcortical infarcts, Subcutaneous hemorrhage, Syringomyelia, Ventricular septal defect, Vulval varicesView all (60 more) |
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293
|
|
|
Notch receptor 4 |
INT3 |
Asthma, Bipolar disorder, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Cryoglobulinemia, Development disorder, Diabetes mellitus, Lung adenocarcinoma, Lung cancer, Lupus erythematosus, Age-related macular degeneration, Marfan syndrome, Multiple sclerosis, Myasthenia gravis, Narcolepsy, Oral ulcer, Pancreatic ductal carcinoma, Pemphigus vulgaris, Rheumatoid arthritis, Sarcoidosis, Schizophrenia, Scleroderma, Skin cancer, Skin neoplasms, VitiligoView all (15 more) |
|
294
|
|
|
Neuronal PAS domain protein 1 |
MOP5, PASD5, bHLHe11 |
|
|
295
|
|
|
Neuronal PAS domain protein 2 |
MOP4, PASD4, bHLHe9 |
|
|
296
|
|
|
NPC intracellular cholesterol transporter 1 |
NPC, POGZ, SLC65A1 |
Apraxia, Atherosclerosis, Cardiovascular diseases, Cataplexy, Coronary artery disease, Dementia, Developmental delay, Dysarthria, Dysphagia, External ophthalmoplegia, Fetal ascites, Gastrointestinal stromal tumor, Impaired cognition, Liver cirrhosis, Liver fibrosis, Mental retardation, Movement disorders, Niemann-pick disease, Obesity, Psychosis, Rubral tremor, Schizophrenia, Sea-blue histiocytosis, Sphingomyelinase deficiency, Supranuclear gaze palsyView all (10 more) |
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297
|
|
|
Nephrocystin 1 |
JBTS4, NPH1, SLSN1 |
Agenesis of corpus callosum, Anemia, Bardet-biedl syndrome, Cataract, Ciliopathies, Congenital cerebral hernia, Congenital coloboma of iris, Congenital hepatic fibrosis, Hypoplasia of the ovary, Congenital hypoplasia of penis, Cryptorchidism, Developmental delay, Disorder of eye, Dwarfism, Hirschsprung disease, Hydrocephalus, Hypertension, Hypogonadism, Impaired cognition, Joubert syndrome, Joubert syndrome with renal defect, Kidney disease, Liver fibrosis, Mental retardation, Multicystic renal dysplasia, Nephronophthisis, Nephrotic syndrome, Nystagmus, Obesity, Oculomotor apraxia, Oculovestibuloauditory syndrome, Polymicrogyria, Premature menopause, Ptosis, Renal corticomedullary cysts, Renal dysplasia and retinal aplasia, Renal insufficiency, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophy, Scoliosis, Senior-loken syndrome, Speech disorders, Strabismus, Syndactyly of fingers, Postaxial hand polydactylyView all (31 more) |
|
298
|
|
|
NPHS1 adhesion molecule, nephrin |
CNF, NPHN, nephrin |
Bright disease, Congenital alveolar dysplasia, Congenital nephrotic syndrome, Finnish congenital nephrotic syndrome, Gastroesophageal reflux disease, Genetic steroid-resistant nephrotic syndrome, Glomerular hyalinosis, Glomerulonephritis, Glomerulosclerosis, Hyperhomocysteinemia, Hyperlipidemia, Hypoalbuminemia, Hypoproteinemia, Hypothyroidism, Kidney disease, Kidney failure, Lipoid nephrosis, Mesangial sclerosis, Nephritis, Nephrosis, congenital, Nephrotic syndrome, Renal glomerular disease, Renal insufficiencyView all (8 more) |
|
299
|
|
|
Nucleophosmin 1 |
B23, NPM |
Anaplastic lymphoma, Anemia, Anorexia, Diffuse alveolar hemorrhage, Disseminated intravascular coagulation, Dyskeratosis congenita, Dyskeratosis congenita, x-linked, Erythroleukemia, Fibrinogen deficiency, Gangrene, Gastric cancer, Hypofibrinogenemia, Leukemia, Leukopenia, Lung adenocarcinoma, Non-hodgkin lymphoma, Lymphomatoid papulosis, Myeloblastic leukemia with maturation, Myeloblastic leukemia without maturation, Myeloid leukemia, Myeloid leukemia with npm1 somatic mutations, Neutropenia, Pancytopenia, Promyelocytic leukemia, Stomach neoplasms, StomatitisView all (11 more) |
|
300
|
|
|
Natriuretic peptide A |
ANF, ANP, ATFB6, ATRST2, CDD, CDD-ANF, CDP, PND |
Adenocarcinoma, Aortic valve insufficiency, Atrial cardiomyopathy, Atrial fibrillation, Atrial standstill, Carcinoma, Cardiomyopathy, Congestive heart failure, Coronary stenosis, Heart failure, Hyperpepsinogenemia, Hypertension, Kidney failure, Left ventricular hypertrophy, Liver cirrhosis, Liver fibrosis, Lung neoplasms, Lung cancer, Melanoma, Myocardial infarction, Myocardial ischemia, Patent ductus arteriosus, Prostatic neoplasms, Prostate cancer, Psoriasis, Acute kidney insufficiency, Renal hypertension, Skin cancer, Skin neoplasms, Stroke, Urination disordersView all (16 more) |
