|
401
|
|
|
Ficolin 3 |
FCNH, HAKA1 |
|
|
402
|
|
|
Family with sequence similarity 193 member A |
C4orf8, RES4-22 |
|
|
403
|
|
|
Fas associated via death domain |
GIG3, IMD90, MORT1 |
Cerebral atrophy, Congenital atresia of pulmonary artery, Dental diseases, Diverticular bleeding, Diverticular diseases, Epileptic encephalopathy, Hearing loss, Howell-jolly bodies, Liver fibrosis, Oculootodental syndrome, Stomatognathic diseases, Ventricular septal defect |
|
404
|
|
|
Fructose-bisphosphatase 2 |
CORLK |
|
|
405
|
|
|
Fucose-1-phosphate guanylyltransferase |
GFPP |
|
|
406
|
|
|
Fibroblast growth factor 18 |
FGF-18, ZFGF5 |
|
|
407
|
|
|
Fibroblast growth factor 17 |
FGF-13, FGF-17, HH20 |
Anxiety disorder, Bipolar disorder, Congenital camptodactyly, Breast hypoplasia, Hypoplasia of the ovary, Congenital sensorineural hearing loss, Cryptorchidism, Dysarthria, Erectile dysfunction, Female hypogonadism syndrome, Gynecomastia, Hearing loss, Hypogonadism, Hypogonadotropic hypogonadism, Hypogonadotropic hypogonadism with or without anosmia, Hypopituitarism, Ichthyosis, Kallmann syndrome, Mental depression, Mirror movements, Non-obstructive azoospermia, Normosmic congenital hypogonadotropic hypogonadism, Nystagmus, Obesity, Osteochondrodysplasia, Osteopenia, Osteoporosis, Paraplegia, Penis agenesis, Physiologic amenorrhea, Ptosis, Renal agenesis, Secondary physiologic amenorrhea, Skeletal dysplasia, Testicular hypogonadismView all (20 more) |
|
408
|
|
|
Fibroblast growth factor 16 |
FGF-16, MF4 |
|
|
409
|
|
|
Fc gamma binding protein |
FC(GAMMA)BP |
|
|
410
|
|
|
Far upstream element binding protein 1 |
FBP, FUBP, hDH V |
|
