|
511
|
|
|
Clavesin 1 |
C6orf212L, CRALBPL, RLBP1L1 |
|
|
512
|
|
|
Cytochrome P450 family 4 subfamily A member 11 |
CP4Y, CYP4A2, CYP4AII, CYPIVA11 |
|
|
513
|
|
|
Calmodulin regulated spectrin associated protein 1 |
CDCBM12 |
|
|
514
|
|
|
Cytochrome P450 family 4 subfamily B member 1 |
CYPIVB1, P-450HP |
|
|
515
|
|
|
Cytochrome P450 family 7 subfamily A member 1 |
CP7A, CYP7, CYPVII |
|
|
516
|
|
|
Cytochrome P450 family 8 subfamily B member 1 |
CP8B, CYP12, CYPVIIIB1 |
|
|
517
|
|
|
Cytochrome P450 family 11 subfamily A member 1 |
CYP11A, CYPXIA1, P450SCC |
46, xy disorder of sex development-adrenal insufficiency, 46, xy disorder of sex development, 46, xy sex reversal, Adrenal calcification, Adrenal insufficiency, congenital, with 46 xy sex reversal, Agenesis of corpus callosum, Atrial septal defect, Clonic seizures, Congenital adrenal insufficiency, with 46,xy sex reversal, partial or complete, Cryptorchidism, Endometrial neoplasms, Endometrial carcinoma, Fetal ascites, Gynecomastia, Hyperaldosteronism, Hypernatriuria, Hypertrophy of clitoris, Hypotonic seizures, Inherited isolated adrenal insufficiency, Jacksonian seizure, Lipoid congenital adrenal hyperplasia, Male pseudohermaphroditism, Hypoglycemia, Osteoporosis, SeizureView all (10 more) |
|
518
|
|
|
Cytochrome P450 family 11 subfamily B member 1 |
CPN1, CYP11B, FHI, P450C11 |
11-beta-hydroxylase deficiency, Adrenal hyperplasia, Adrenogenital syndrome, Ambiguous genitalia, Congenital adrenal hyperplasia, Conn syndrome, Cryptorchidism, Dwarfism, Ectopic adrenal gland, Enlarged polycystic ovaries, Female sexual dysfunction, Gynecomastia, Hyperaldosteronism, Hypernatriuria, Hypertension, Hypertrophy of clitoris, Hypoplasia of vagina, Osteoporosis, Premature adrenarche, Secretory adrenocortical adenoma, StrokeView all (6 more) |
|
519
|
|
|
Cytochrome P450 family 11 subfamily B member 2 |
ALDOS, CPN2, CYP11B, CYP11BL, CYPXIB2, P-450C18, P450C18, P450aldo |
Adrenal hyperplasia, Cardiovascular diseases, Congenital adrenal hyperplasia, Conn syndrome, Corticosterone methyl oxidase deficiency, Hyperaldosteronism, Hypertension, Hypoaldosteronism, Prostatic neoplasms, Prostate cancer, Renal tubular acidosis, Secretory adrenocortical adenoma |
|
520
|
|
|
Cytochrome P450 family 17 subfamily A member 1 |
CPT7, CYP17, P450C17, S17AH |
17,20-lyase deficiency, 46, xy disorder of sex development, Adrenal hyperplasia, Adrenal hyperplasia, congenital, Adrenogenital syndrome, Ambiguous genitalia, Anxiety disorder, Bartter syndrome, Breast cancer, Mammary neoplasms, Breast carcinoma, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Congenital adrenal hyperplasia, Coronary heart disease, Corpus luteum cyst, Cryptorchidism, Dwarfism, Enlarged polycystic ovaries, Frigidity, Gynecomastia, Hyperaldosteronism, Hypertension, Hypoactive sexual desire disorder, Hypogonadism, Hypogonadotropic hypogonadism, Hypokalemia, Hypopituitarism, Hypoplasia of vagina, Hypospadias, Liver carcinoma, Male pseudohermaphroditism, Malignant hypertension, Marfan syndrome, Myocardial infarction, Non-alcoholic fatty liver disease, Orgasmic disorder, Osteoporosis, Ovarian cysts, Parkinson disease, Penis agenesis, Physiologic amenorrhea, Prostatic neoplasms, Prostate cancer, Psychosexual disorders, Sexual arousal disorder, Sheehan syndrome, SubfertilityView all (34 more) |
