|
111
|
|
|
NudC domain containing 3 |
NudCL |
|
|
112
|
|
|
Non-SMC condensin I complex subunit H |
BRRN1, CAP-H, CAPH, MCPH23, NCAPH1 |
|
|
113
|
|
|
Neuronal calcium sensor 1 |
FLUP, FREQ |
|
|
114
|
|
|
Nicotinamide nucleotide transhydrogenase |
GCCD4 |
Adrenal hypoplasia, x-linked, Anorexia, Azoospermia, Chronic obstructive pulmonary disease, Congenital hypothyroidism, Cryptorchidism, Glucocorticoid deficiency, Glucocorticoid deficiency with or without mineralocorticoid deficiency, Glucocorticoid deficiency with mineralocorticoid deficiency, Hypernatriuria, Hypertrophic cardiomyopathy, Hypoglycemia, Hypoglycemic coma, Hypoglycemic seizures, Mental retardation, Precocious puberty, Quadriplegia, Testicular adrenal rest tumorView all (3 more) |
|
115
|
|
|
Nucleoporin 62 |
IBSN, SNDI, p62 |
Basal ganglia cysts, Choreoathetosis, Developmental regression, Dysarthria, Dysphagia, Gastroesophageal reflux disease, Horizontal pendular nystagmus, Mental retardation, Optic atrophy, Pendular nystagmus, Spastic tetraparesis, Striatal necrosis, Striatonigral degeneration |
|
116
|
|
|
Nuclear pore associated protein 1 |
C15orf2 |
Acromicria, Acromicric dysplasia, Attention deficit hyperactivity disorder, Clinodactyly, Colorectal cancer, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Hyperinsulinism, Hyperopia, Hypogonadotropic hypogonadism, Isolated somatotropin deficiency, Melanoma, Motor delay, Hypotonia, Penis agenesis, Physiologic amenorrhea, Prader-willi syndrome, Royer syndrome, Scoliosis, Sleep apnea, Somatotropin deficiency, Specific learning disorderView all (9 more) |
|
117
|
|
|
Nuclear receptor subfamily 5 group A member 2 |
B1F, B1F2, CPF, FTF, FTZ-F1, FTZ-F1beta, LRH-1, LRH1, hB1F-2 |
Ankylosing spondylitis, Cholangitis, Crohn disease, Dyslipidemias, Inflammatory bowel disease, Nasopharyngeal carcinoma, Non-alcoholic fatty liver disease, Pancreatic neoplasm, Pancreatic carcinoma, Pancreatic cancer, Psoriasis, Subfertility, Ulcerative colitis |
|
118
|
|
|
Nuclear receptor subfamily 5 group A member 1 |
AD4BP, ELP, FTZ1, FTZF1, POF7, SF-1, SF1, SPGF8, SRXX4, SRXY3, hSF-1 |
46, xx gonadal dysgenesis, 46, xx ovotesticular disorder of sex development, 46, xx gonadal sex reversal, 46, xy complete gonadal dysgenesis, 46, xy disorder of sex development, 46, xy partial gonadal dysgenesis, 46, xy sex reversal, 46,xx gonadal dysgenesis, Adrenal cortical hypofunction, Adrenal hypoplasia, x-linked, Adrenal insufficiency, Ambiguous genitalia, Arachnodactyly, Azoospermia, Congenital hypoplasia of penis, Cryptorchidism, Dwarfism, Endometrioma, Endometriosis, Gonadal dysgenesis, Gonadotropin-resistant ovary syndrome, Gynecomastia, Hypertrophy of clitoris, Hypogonadism, Hypogonadotropic hypogonadism, Hypoplasia of vagina, Hypospadias, Male infertility, Male pseudohermaphroditism, Microcephaly, Nephroblastoma, Nephrotic syndrome, Non-obstructive azoospermia, Obstructive azoospermia, Oligosynaptic infertility, Osteopenia, Osteoporosis, Osteoporosis of vertebrae, Ovarian neoplasm, Ovarian cancer, Ovarian failure, Ovarian gonadoblastoma, Penis agenesis, Physiologic amenorrhea, Polycystic ovary syndrome, Premature menopause, Premature ovarian failure, Pulmonary fibrosis, Secondary physiologic amenorrhea, Spermatogenic failure, Streak ovary, Swyer syndrome, Testicular dysgenesis, Testicular gonadoblastoma, Testicular hypogonadism, Testicular regression syndrome, True hermaphroditism, Uterine anomalies, Xx malesView all (44 more) |
|
119
|
|
|
NIFK antisense RNA 1 |
- |
|
|
120
|
|
|
N-acetylated alpha-linked acidic dipeptidase like 2 |
- |
|
