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51
|
|
|
Nucleus accumbens associated 1 |
BEND8, BTBD14B, BTBD30, NAC-1, NAC1, NECFM |
Benign neoplasm, Brachycephaly, Camptodactyly of fingers, Cataract, Cerebral atrophy, Congenital pectus excavatum, Developmental delay, Infantile spasms, Malignant neoplasm, Mental retardation, Microcephaly, Myoclonic seizures, Neoplasms, Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination, Neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract, Oropharyngeal dysphagia, Scoliosis, Sleep apnea, Stereotyped behaviorView all (4 more) |
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52
|
|
|
NLR family pyrin domain containing 3 |
AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1, DFNA34, FCAS, FCAS1, FCU, KEFH, MWS, NALP3, PYPAF1 |
Acne, Amyloid nephropathy, Anemia, Aphthous ulcer, Arthritis, Asbestosis, Autoinflammatory disease, Brachydactyly, Cinca syndrome, Cold autoinflammatory syndrome, Cold urticaria, Congenital anomaly of nose, Conjunctivitis, Cranial nerve paralysis, Crohn disease, Crohn`s disease of large bowel, Crohn`s disease of the ileum, Cryopyrin-associated periodic syndromes, Deafness, Developmental delay, Dwarfism, Episcleritis, Excessive tearing, Frontal bossing, Glaucoma, Hearing loss, Hernia of abdominal wall, Hidradenitis suppurativa, Ichthyosis, Ileocolitis, Keratitis, Keratitis fugax hereditaria, Kidney disease, Macrocephaly, Mental retardation, Migraine, Mouth abnormalities, Muckle-wells syndrome, Multiple sclerosis, Nephrotic syndrome, Neurological, cutaneous and articular syndrome, Optic atrophy, Osteochondrodysplasia, Pericardial effusion, Pleural effusion, Proptosis, Pseudopapilledema, Pyoderma gangrenosum, Renal insufficiency, Retrobulbar neuritis, Skeletal dysplasia, Talipes transversoplanus, Urticaria, Uveitis, VasculitisView all (40 more) |
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53
|
|
|
NUS1 dehydrodolichyl diphosphate synthase subunit |
C6orf68, CDG1AA, MGC:7199, MRD55, NgBR, TANGO14 |
Attention deficit hyperactivity disorder, Autism, Cerebral atrophy, Cerebral cortical atrophy, Congenital disorder of glycosylation, Developmental delay, Developmental regression, Diabetes mellitus, Dwarfism, Dyskinetic syndrome, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypertrichosis, Hypodontia, Melanoma, Mental retardation, Microcephaly, Myoclonic seizures, Non-specifi epileptic encephalopathy, Nystagmus, Optic atrophy, Ptosis, Scoliosis, Status epilepticusView all (9 more) |
|
54
|
|
|
Niban apoptosis regulator 1 |
C1orf24, FAM129A, GIG39, NIBAN |
|
|
55
|
|
|
Neurexophilin and PC-esterase domain family member 1 |
FAM55A |
|
|
56
|
|
|
Non-coding RNA in the aldehyde dehydrogenase 1A pathway |
LINC00284, NCRNA00284 |
|
|
57
|
|
|
NIPA magnesium transporter 1 |
FSP3, SLC57A1, SPG6 |
|
|
58
|
|
|
N-terminal asparagine amidase |
PNAA, PNAD |
|
|
59
|
|
|
NLR family pyrin domain containing 8 |
CLR19.2, NALP8, NOD16, PAN4 |
|
|
60
|
|
|
NADH:ubiquinone oxidoreductase subunit A11 |
B14.7, CI-B14.7, MC1DN14 |
Brain atrophy, Cerebral atrophy, Developmental delay, Diabetes mellitus, Epileptic encephalopathy, Hearing loss, Hypertrophic cardiomyopathy, Hypoglycemia, Isolated complex i deficiency, Leukodystrophy, Leukoencephalopathy, Microcephaly, Mitochondrial complex deficiency, Mitochondrial diseases, Mitochondrial myopathy, Myopathy, Nystagmus, Optic atrophy, Ptosis, StrabismusView all (5 more) |
