|
331
|
|
|
Follistatin like 5 |
- |
|
|
332
|
|
|
Fem-1 homolog C |
EUROIMAGE686608, EUROIMAGE783647, FEM1A |
|
|
333
|
|
|
FAM20C golgi associated secretory pathway kinase |
DMP-4, DMP4, G-CK, GEF-CK, RNS |
Choanal atresia, Mandibular aplasia, Pulmonary hypoplasia, Cortical dysplasia, Developmental delay, Dwarfism, High palate, Microcephaly, Micrognathism, Microstomia, Osteosclerosis, Osteosclerotic bone dysplasia, Posteriorly rotated ear, Proptosis, Raine syndrome, Respiratory failure, Thoracic hypoplasiaView all (2 more) |
|
334
|
|
|
Fibrosin like 1 |
- |
|
|
335
|
|
|
FA complementation group M |
FAAP250, KIAA1596, POF15, SPGF28 |
Anemia, Astigmatism, Atrial septal defect, Azoospermia, Cafe-au-lait spot, Camptodactyly of fingers, Cataract, Choanal atresia, Congenital arteriovenous malformation, Congenital epicanthus, Congenital exomphalos, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Fanconi anemia, Frontal bossing, High palate, Hirschsprung disease, Hydrocephalus, Hypertrophic cardiomyopathy, Hypogonadism, Hypospadias, Imperforate anus, Leukemia, Leukopenia, Male infertility, Head and neck cancer, Malignant ovarian germ cell neoplasm, Meckel diverticulum, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Miller dieker syndrome, Monocytic leukemia, Myelodysplasia, Myelodysplastic syndrome, Non-obstructive azoospermia, Nystagmus, Obstructive azoospermia, Ovarian neoplasm, Pancytopenia, Patent ductus arteriosus, Premature ovarian failure, Proptosis, Ptosis, Renal insufficiency, Retinoblastoma, Scoliosis, Spermatogenic failure, Spina bifida, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Tetralogy of fallotView all (42 more) |
|
336
|
|
|
FHF complex subunit HOOK interacting protein 2A |
FAM160B1, KIAA1600, bA106M7.3 |
|
|
337
|
|
|
FAST kinase domains 5 |
dJ1187M17.5 |
|
|
338
|
|
|
FKBP prolyl isomerase 10 |
BRKS, BRKS1, FKBP65, OI11, OI6, PPIASE, TLH1, hFKBP65 |
Acquired kyphoscoliosis, Arthrogryposis multiplex congenita, Brachycephaly, Bruck syndrome, Congenital clubfoot, Congenital kyphoscoliosis, Congenital pectus carinatum, Dentinogenesis imperfecta, Dwarfism, Elbow flexion contracture, Hip contracture, Kuskokwim syndrome, Melanocytic nevus, Multiple congenital anomalies, Osteogenesis imperfecta, Osteopenia, Osteoporosis, Pterygium, Scoliosis, TalipesView all (5 more) |
|
339
|
|
|
FAM111 trypsin like peptidase A |
GCLEB, KCS2 |
Anemia, Aniridia, Ankyloglossia, Brachydactyly, Congenital hypoparathyroidism, Defect of skull ossification, Developmental delay, Disorder of macula of retina, Dwarfism, Gracile bone dysplasia, Hydrocephalus, Hyperopia, Hyperphosphatemia, Hypocalcemic seizures, Hypocalcemic tetany, Hypoparathyroidism, Kenny-caffey syndrome, Macrocephaly, Microphthalmos, Osteocraniostenosis, Osteosclerosis, Papilledema, Penis agenesis, Stenosis of the medullary cavity of the long bonesView all (9 more) |
|
340
|
|
|
Family with sequence similarity 217 member B |
C20orf177, dJ551D2.5 |
|
