|
411
|
|
|
Non-coding RNA activated by DNA damage |
LINC00657 |
|
|
412
|
|
|
Nicotinamide nucleotide adenylyltransferase 1 |
LCA9, NMNAT, PNAT1, SHILCA |
Cataract, Coloboma of macula, Cone dystrophy, Cone-rod dystrophy, Dysgenesis neuroepithelialis retinae, Congenital cerebral hernia, Developmental delay, Developmental regression, Hemiplegia/hemiparesis, Hyperopia, Keratoconus, Leber congenital amaurosis, Age-related macular degeneration, Malformation of cortical development, Mental retardation, Nyctalopia, Nystagmus, Optic atrophy, Retinal dystrophyView all (4 more) |
|
413
|
|
|
Nucleic acid binding protein 1 |
NABP1-OT1, OBFC2A, SOSS-B2, SSB2 |
Anemia, Anorexia, Diffuse alveolar hemorrhage, Disseminated intravascular coagulation, Fibrinogen deficiency, Gangrene, Hypofibrinogenemia, Leukopenia, Neutropenia, Pancytopenia, Promyelocytic leukemia, Stomatitis |
|
414
|
|
|
5'-nucleotidase domain containing 2 |
- |
|
|
415
|
|
|
NDRG family member 4 |
BDM1, SMAP-8, SMAP8 |
|
|
416
|
|
|
Neurobeachin like 1 |
A530083I02Rik, ALS2CR16, ALS2CR17 |
|
|
417
|
|
|
Neutrophil cytosolic factor 1 |
CGD1, NCF-1, NCF-47K, NCF1A, NOXO2, SH3PXD1A, p47-phox, p47phox |
Aortic aneurysm, Brain aneurysm, Cerebral aneurysm, Cerebral artery aneurysm, Chronic obstructive pulmonary disease, Diabetes mellitus, Eczema, Giant intracranial aneurysm, Gingivitis, Granulomatosis, Granulomatous disease, Hypercholesterolemia, Hypertension, Hypertrophic cardiomyopathy, Immunologic deficiency syndromes, Inflammatory abnormality of the eye, Intracranial aneurysm, Kidney failure, Lupus erythematosus, Lymphadenitis, Malabsorption syndrome, Mediastinal lymphadenopathy, Mycotic aneurysm, intracranial, Nonbacterial verrucal endocardiosis, Osteomyelitis, Otitis media, Posterior communicating artery aneurysm, Rheumatoid arthritis, Sjogren`s syndrome, SinusitisView all (15 more) |
|
418
|
|
|
- |
- |
Addison`s disease, Wolff-parkinson-white syndrome, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Cardiomyopathy, Cataract, Central visual impairment, Cerebral cortical atrophy, Congestive heart failure, Dementia, Demyelinating neuropathy, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Dyskinetic syndrome, Dysphagia, Epileptic encephalopathy, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hereditary leber optic atrophy, Hereditary optic atrophy, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Intestinal obstruction, Leber plus disease, Left ventricular hypertrophy, Leigh syndrome, Liver failure, Malabsorption syndrome, Malformation of cortical development, Maternally inherited leigh syndrome, Melas syndrome, Mental depression, Microcephaly, Migraine, Mitochondrial myopathy, Multiple lipomata, Myoclonic seizures, Myopathy, Nephrotic syndrome, Nervous system diseases, Nyctalopia, Nystagmus, Optic atrophy, Oxyphilic adenoma, Pancreatitis, Parkinson disease, Polyneuropathy, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Retinal telangiectasia, Retinitis pigmentosa, Rod-cone dystrophy, Seizure, Sensorimotor neuropathy, Sensorineural hearing loss, Thyroiditis, Ventricular preexcitation, West syndromeView all (63 more) |
|
419
|
|
|
- |
- |
Addison`s disease, Wolff-parkinson-white syndrome, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Cardiomyopathy, Cataract, Central visual impairment, Cerebral cortical atrophy, Congestive heart failure, Dementia, Demyelinating neuropathy, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Dyskinetic syndrome, Dysphagia, Epileptic encephalopathy, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hereditary leber optic atrophy, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Impaired cognition, Intestinal obstruction, Left ventricular hypertrophy, Leigh syndrome, Liver failure, Malabsorption syndrome, Malformation of cortical development, Maternally inherited leigh syndrome, Melas syndrome, Mental depression, Merrf syndrome, Microcephaly, Migraine, Mitochondrial diseases, Mitochondrial myopathy, Movement disorders, Multiple lipomata, Myoclonic seizures, Myopathy, Nephrotic syndrome, Nervous system diseases, Nyctalopia, Nystagmus, Optic atrophy, Pancreatitis, Polyneuropathy, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Retinal telangiectasia, Retinitis pigmentosa, Rod-cone dystrophy, Seizure, Sensorimotor neuropathy, Sensorineural hearing loss, Thyroiditis, Ventricular preexcitation, West syndromeView all (63 more) |
|
420
|
|
|
- |
- |
|
