|
201
|
|
|
NLR family apoptosis inhibitory protein |
BIRC1, NLRB1, psiNAIP |
|
|
202
|
|
|
NBL1, DAN family BMP antagonist |
D1S1733E, DAN, DAND1, NB, NO3 |
|
|
203
|
|
|
Nibrin |
AT-V1, AT-V2, ATV, NBS, NBS1, P95, hNbs1 |
Aplastic anemia, Attention deficit hyperactivity disorder, Autoimmune hemolytic anemia, B-cell lymphoma, Breast cancer, Breast carcinoma, Bronchiectasis, Bronchitis, Hereditary cancer syndrome, Choanal atresia, Dwarfism, Dysgammaglobulinemia, Endometrial carcinoma, Glioma, Hereditary breast and ovarian cancer syndrome, Hydronephrosis, Hypoplastic anemia, Imperforate anus, Lymphoblastic leukemia, Leukemia, Lissencephaly, Lymphocytic leukemia, Lymphoma, Non-hodgkin lymphoma, Macrotia, Malformation of cortical development, Mastoiditis, Medulloblastoma, Melanoma, Mental retardation, Microcephaly, Micrognathism, Nicolaides baraitser syndrome, Nijmegen breakage syndrome, Oral mucositis, Otitis media, Ovarian neoplasm, Ovarian cancer, Pancreatic neoplasm, Peritoneal carcinoma, Premature menopause, Prostatic neoplasms, Prostate cancer, Respiratory failure, Rhabdomyosarcoma, Sinusitis, Stomatitis, T-cell lymphomaView all (33 more) |
|
204
|
|
|
Neural cell adhesion molecule 1 |
CD56, MSK39, NCAM |
|
|
205
|
|
|
Neural cell adhesion molecule 2 |
NCAM21 |
|
|
206
|
|
|
Neutrophil cytosolic factor 2 |
NCF-2, NOXA2, P67-PHOX, P67PHOX |
Celiac disease, Chronic obstructive pulmonary disease, Eczema, Gingivitis, Granulomatosis, Granulomatous disease, Immunologic deficiency syndromes, Inflammatory abnormality of the eye, Lupus erythematosus, Lymphadenitis, Malabsorption syndrome, Mediastinal lymphadenopathy, Myositis, Osteomyelitis, Otitis media, Rheumatoid arthritis, Scleroderma, SinusitisView all (3 more) |
|
207
|
|
|
Neutrophil cytosolic factor 4 |
CGD3, NCF, P40PHOX, SH3PXD4 |
Aphthous ulcer, Chronic obstructive pulmonary disease, Colitis, Crohn disease, Crohn`s disease of large bowel, Crohn`s disease of the ileum, Eczema, Gingivitis, Granulomatous disease, Heart diseases, Ileocolitis, Inflammatory abnormality of the eye, Malabsorption syndrome, Mediastinal lymphadenopathy, Otitis media, Perioral eczema, SinusitisView all (2 more) |
|
208
|
|
|
NCK adaptor protein 1 |
NCK, NCKalpha, nck-1 |
|
|
209
|
|
|
Nucleolin |
C23, Nsr1 |
|
|
210
|
|
|
Necdin, MAGE family member |
HsT16328, PWCR |
Acromicria, Acromicric dysplasia, Anaplastic carcinoma, Attention deficit hyperactivity disorder, Carcinoma, Clinodactyly, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Hyperinsulinism, Hyperopia, Hypogonadotropic hypogonadism, Isolated somatotropin deficiency, Motor delay, Hypotonia, Penis agenesis, Physiologic amenorrhea, Prader-willi syndrome, Royer syndrome, Scoliosis, Sleep apnea, Somatotropin deficiency, Specific learning disorderView all (9 more) |
