31
|
|
|
Bromodomain adjacent to zinc finger domain 1A |
ACF1, WALp1, WCRF180, hACF1 |
|
32
|
|
|
Beta-1,4-galactosyltransferase 7 |
EDSP1, EDSSLA, EDSSPD1, XGALT1, XGPT, XGPT1 |
Acquired kyphoscoliosis, Aortic valve sclerosis, Arachnodactyly, Congenital epicanthus, Short clavicles, Congenital kyphoscoliosis, Congenital pectus carinatum, Cryptorchidism, Cutis laxa, Developmental delay, Dwarfism, Ehlers-danlos syndrome, Gingivitis, Larsen syndrome, Lipodystrophy, Macrocephaly, Microstomia, Osteochondrodysplasia, Osteopenia, Proptosis, Pulmonary stenosis, Radioulnar synostosis, Skeletal dysplasia, Spermatic cord torsion, Spondylodysplastic ehlers-danlos syndromeView all (10 more) |
33
|
|
|
BTB domain containing 9 |
dJ322I12.1 |
|
34
|
|
|
Basic leucine zipper ATF-like transcription factor 2 |
SARI |
|
35
|
|
|
BLOC-1 related complex subunit 5 |
LOH12CR1, LOH1CR12 |
|
36
|
|
|
BLOC-1 related complex subunit 7 |
C10orf32 |
|
37
|
|
|
Beta-1,4-N-acetyl-galactosaminyltransferase 2 (SID blood group) |
B4GALT, GALGT2 |
|
38
|
|
|
Beta-1,3-galactosyltransferase 6 |
ALGAZ, EDSP2, EDSSPD2, SEMDJL1, beta3GalT6 |
Acquired kyphoscoliosis, Atrial septal defect, Bicuspid aortic valve, Congenital clubfoot, Dislocated radial head, Congenital kyphoscoliosis, Cutis laxa, Developmental delay, Dwarfism, Ectopia lentis, Ehlers-danlos syndrome, Epiphyseal dysplasia, Heart septal defects, High palate, Hirschsprung disease, Mental retardation, Micrognathism, Micromelia, Myopia, Osteoporosis, Paraplegia, Proptosis, Scoliosis, Spinal cord compression, Spondylodysplastic ehlers-danlos syndrome, Spondyloepimetaphyseal dysplasia, Spondyloepimetaphyseal dysplasia with joint laxity, Ventricular septal defectView all (13 more) |
39
|
|
|
BPI fold containing family A member 3 |
C20orf71, SPLUNC3 |
|
40
|
|
|
Bardet-Biedl syndrome 5 |
- |
Bardet-biedl syndrome, Brachydactyly, Ciliopathies, Cone dystrophy, Hypoplasia of the ovary, Congenital hypoplasia of penis, Cryptorchidism, Diastrophic dysplasia, Disorder of eye, Dwarfism, Hypertension, Hypogonadism, Impaired cognition, Keratosis follicularis, Liver fibrosis, Age-related macular degeneration, Mental retardation, Multicystic renal dysplasia, Nephrotic syndrome, Nystagmus, Obesity, Polydactyly, Retinitis pigmentosa, Rod-cone dystrophy, Speech disorders, Syndactyly, Syndactyly of fingers, Postaxial hand polydactylyView all (13 more) |