|
391
|
|
|
Neuroglobin |
- |
|
|
392
|
|
|
Nectin cell adhesion molecule 1 |
CD111, CLPED1, ED4, HIgR, HV1S, HVEC, OFC7, PRR, PRR1, PVRL1, PVRR, PVRR1, SK-12, nectin-1 |
Alopecia, Anodontia, Cleft lip with or without cleft palate, Cleft lip/palate-ectodermal dysplasia syndrome, Cleft palate and bilateral cleft lip, Congenital abnormality of eustachian tube, Congenital clubfoot, Congenital exomphalos, Dysphagia, Ectodermal dysplasia, Hearing loss, Hypodontia, Hypogonadism, Hypohidrosis, Hypoplasia of the maxilla, Macrodontia, Macrotia, Malnutrition, Mental retardation, Microdontia, Micrognathism, Nail diseases, Nail dysplasia, Obsessive-compulsive disorder, Oropharyngeal dysphagia, Orofacial cleft, Otitis media, Palmoplantar keratosis, Situs inversus, Specific learning disorder, Speech disorders, Syndactyly of fingers, Syndactyly of the toes, Synophrys, Tourette syndrome, Velopharyngeal insufficiencyView all (21 more) |
|
393
|
|
|
Nectin cell adhesion molecule 2 |
CD112, HVEB, PRR2, PVRL2, PVRR2 |
Alzheimer disease, Atherosclerosis, Urinary bladder cancer, Bladder neoplasm, Breast cancer, Mammary neoplasms, Breast carcinoma, Cerebral amyloid angiopathy, Cognitive disorder, Dementia, Diabetes mellitus, Diffuse lymphoma, Dyslipidemias, Impaired cognition, Leukemia, Age-related macular degeneration, Marfan syndrome, Multiple sclerosis, Myeloid leukemia, Orofacial cleft, Ovarian neoplasm, Ovarian cancer, Parkinson disease, Prostatic neoplasms, Prostate cancer, Scleroderma, Senile dementia, T-cell lymphoma, TeratozoospermiaView all (14 more) |
|
394
|
|
|
NLR family CARD domain containing 4 |
AIFEC, CARD12, CLAN, CLAN1, CLANA, CLANB, CLANC, CLAND, CLR2.1, FCAS4, IPAF |
Anemia, Arthritis, Autoinflammation with enterocolitis, Autoinflammatory disease, Brachydactyly, Breast carcinoma, Cold autoinflammatory syndrome, Cold urticaria, Conjunctivitis, Cryopyrin-associated periodic syndromes, Developmental delay, Disseminated intravascular coagulation, Dwarfism, Enterocolitis, Frontal bossing, Hearing loss, Macrocephaly, Macrophage activation syndrome, Mental retardation, Migraine, Muckle-wells syndrome, Neurological, cutaneous and articular syndrome, Osteochondrodysplasia, Pancytopenia, Proptosis, Pseudopapilledema, Retrobulbar neuritis, Skeletal dysplasia, Urticaria, UveitisView all (15 more) |
|
395
|
|
|
Netrin 4 |
PRO3091 |
|
|
396
|
|
|
Neuropeptide S |
- |
|
|
397
|
|
|
Nyctalopin |
CLRP, CSNB1, CSNB1A, CSNB4, NBM1 |
Congenital stationary night blindness, Disorder of eye, Hemeralopia, Hypoplasia of optic disc, Myopia, Night blindness, Nyctalopia, Nystagmus, Strabismus, Congenital stationary night blindness, x-linked |
|
398
|
|
|
Neuronal differentiation 6 |
Atoh2, MATH2, Math-2, NEX1M, Nex1, bHLHa2 |
|
|
399
|
|
|
Neuronal PAS domain protein 3 |
MOP6, PASD6, bHLHe12 |
|
|
400
|
|
|
Nucleotide binding oligomerization domain containing 2 |
ACUG, BLAU, BLAUS, CARD15, CD, CLR16.3, IBD1, NLRC2, NOD2B, PSORAS1, YAOS |
Acne, Anemia, Ankylosing spondylitis, Aortic aneurysm, Aphthous ulcer, Arthritis, Arthrocutaneouveal granulomatosis, Asthma, Autoinflammatory disease, Behcet syndrome, Bipolar disorder, Blau syndrome, Cataract, Cholangitis, Corneal dystrophy, Crohn disease, Crohn`s disease of large bowel, Crohn`s disease of the ileum, Cystoid macular edema, Dermatitis, Eczema, Erythema nodosum, Facial paralysis, Glaucoma, Hidradenitis suppurativa, Hypertension, Ichthyosis, Ileocolitis, Inflammatory bowel disease, Intestinal obstruction, Iridocyclitis, Iritis, Keratitis, Keratoconjunctivitis sicca, Kidney disease, Nephrolithiasis, Nongranulomatous uveitis, Oral ulcer, Pericarditis, Pleuritis, Polyarthritis, Psoriasis, Psoriatic arthritis, Pulmonary arterial hypertension, Pyoderma gangrenosum, Renal carcinoma, Retinal diseases, Retrobulbar neuritis, Sarcoidosis, Synovitis, Tendinitis, Ulcerative colitis, Uveitis, Vasculitis, Ventricular hypertrophy, Yao syndromeView all (41 more) |
