|
3211
|
|
|
LHFPL tetraspan subfamily member 5 |
DFNB67, TMHS, dJ510O8.8 |
|
|
3212
|
|
|
Zinc finger and SCAN domain containing 23 |
ZNF390, ZNF453, dJ29K1.3, dJ29K1.3.1 |
|
|
3213
|
|
|
NFKB activating protein like |
C6orf194, bA424I5.1 |
|
|
3214
|
|
|
Fer3 like bHLH transcription factor |
N-TWIST, NATO3, NTWIST, PTFB, bHLHa31 |
|
|
3215
|
|
|
ITPR interacting domain containing 1 |
CCDC129 |
|
|
3216
|
|
|
Semaphorin 3D |
Sema-Z2, coll-2 |
|
|
3217
|
|
|
Ferredoxin reductase |
ADR, ADXR, ANOA, MMDS9B |
|
|
3218
|
|
|
Ferrochelatase |
EPP, EPP1, FCE |
|
|
3219
|
|
|
Flap structure-specific endonuclease 1 |
FEN-1, MF1, RAD2 |
|
|
3220
|
|
|
Glypican 4 |
K-glypican, KPTS |
Abnormal spinal segmentation, Accessory nipple, Agenesis of corpus callosum, Atrial septal defect, Brachydactyly, Bundle branch block, Camptodactyly of fingers, Cardiomyopathy, Clinodactyly, Congenital clubfoot, Congenital diaphragmatic hernia, Developmental dysplasia of the hip, Congenital epicanthus, Congenital exomphalos, Congenital hypoplasia of penis, Congenital malrotation of intestine, Congenital omphalocele, Congenital pectus excavatum, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Double ureter, Dwarfism, Hearing loss, Hepatoblastoma, Hydrocephalus, Hydronephrosis, Hypoglycemia, Hypoplasia of the maxilla, Hypospadias, Impaired cognition, Keipert syndrome, Macrocephaly, Macroglossia, Macrostomia, Malocclusion, Meckel diverticulum, Mental retardation, Multicystic renal dysplasia, Nail diseases, Nail dysplasia, Nasodigitoacoustic syndrome, Neck webbing, Nephroblastoma, Neuroblastoma, Patent ductus arteriosus, Polydactyly, Polysplenia, Ptosis, Pulmonary stenosis, Renal cyst, Scoliosis, Simpson-golabi-behmel syndrome, Spade-like hand, Speech disorders, Syndactyly of fingers, Syndactyly of the toes, Talipes transversoplanus, Transposition of great vessels, Postaxial hand polydactyly, Ventricular septal defect, Wilms tumorView all (47 more) |
