|
311
|
|
|
FXYD domain containing ion transport regulator 3 |
MAT8, PLML |
|
|
312
|
|
|
FXYD domain containing ion transport regulator 6 |
- |
|
|
313
|
|
|
Fibroblast growth factor receptor like 1 |
FGFR-5, FGFR5, FHFR |
Absence of septum pellucidum, Axenfeld anomaly, Congenital anomaly of eye, Congenital clubfoot, Congenital diaphragmatic hernia, Congenital epicanthus, Rib fusion, Posterolateral diaphragmatic hernia, Morgagni diaphragmatic hernia, Cryptorchidism, Developmental delay, Dwarfism, Gastroesophageal reflux disease, Hemangioma, Hypodontia, Hypospadias, Immunologic deficiency syndromes, Mental retardation, Microcephaly, Micrognathism, Nystagmus, Pitt-rogers-danks syndrome, Precocious puberty, Proptosis, Ptosis, Radioulnar synostosis, Rieger syndrome, Scoliosis, Stenosis of external auditory canal, Stereotyped behavior, Strabismus, Ventricular septal defect, Wolf-hirschhorn syndromeView all (18 more) |
|
314
|
|
|
F-box and WD repeat domain containing 11 pseudogene 1 |
BTRC2P, FBXW1BP, FBXW1BP1 |
|
|
315
|
|
|
F-box and leucine rich repeat protein 19 |
CXXC11, Fbl19, JHDM1C |
|
|
316
|
|
|
FEV transcription factor, ETS family member |
HSRNAFEV, PET-1 |
|
|
317
|
|
|
Filamin binding LIM protein 1 |
CAL, FBLP-1, FBLP1 |
|
|
318
|
|
|
FAM20A golgi associated secretory pathway pseudokinase |
AI1G, AIGFS, FP2747 |
Amelogenesis imperfecta, Arthritis, Enamel-renal syndrome, Juvenile arthritis, Kidney disease, Nephrocalcinosis, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Renal insufficiency, Still disease |
|
319
|
|
|
Family with sequence similarity 118 member A |
C22orf8 |
|
|
320
|
|
|
FKBP prolyl isomerase 14 |
EDSKMH, EDSKSCL2, FKBP22, IPBP12 |
Acquired kyphoscoliosis, Congenital kyphoscoliosis, Congenital muscular dystrophy, Ehlers-danlos syndrome, Kyphoscoliotic ehlers-danlos syndrome, Hearing loss, High-frequency sensorineural hearing impairment, Microcornea, Motor delay, Myopathy, Myopia, Osteopenia, Phrynoderma, Rupture of artery, Thoracolumbar scoliosis |
