|
2471
|
|
|
Cytochrome P450 family 7 subfamily A member 1 |
CP7A, CYP7, CYPVII |
|
|
2472
|
|
|
Tubulin tyrosine ligase like 11 |
C9orf148, C9orf20, TTLL11-IT1, bA244O19.1 |
|
|
2473
|
|
|
Cytochrome P450 family 8 subfamily B member 1 |
CP8B, CYP12, CYPVIIIB1 |
|
|
2474
|
|
|
Tetratricopeptide repeat domain 39B |
C9orf52 |
|
|
2475
|
|
|
Family with sequence similarity 120 member A opposite strand |
C9orf10OS |
|
|
2476
|
|
|
Stabilizer of axonemal microtubules 1 |
C9orf138, FAM154A |
|
|
2477
|
|
|
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) |
|
2478
|
|
|
Long intergenic non-protein coding RNA 475 |
C9orf44 |
|
|
2479
|
|
|
FRAS1 related extracellular matrix 1 |
BNAR, C9orf143, C9orf145, C9orf154, MOTA, TILRR, TRIGNO2 |
Acrocephaly, Bifid nose with or without anorectal and renal anomalies, Bnar syndrome, Brachycephaly, Cardiovascular diseases, Congenital diaphragmatic hernia, Posterolateral diaphragmatic hernia, Morgagni diaphragmatic hernia, Congenital omphalocele, Craniosynostosis, Cryptophthalmos, Disorder of eye, Marles greenberg persaud syndrome, Metopic synostosis, Microphthalmos, Multicystic renal dysplasia, Oculotrichoanal syndrome, Renal agenesis, Renal aplasia, Scaphocephaly, Syndromic microphthalmia, Synophrys, Synostotic anterior plagiocephaly, Synostotic posterior plagiocephaly, TrigonocephalyView all (10 more) |
|
2480
|
|
|
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) |
