241
|
|
|
BR serine/threonine kinase 2 |
C11orf7, PEN11B, SAD-A, SAD1, SADA, STK29 |
|
242
|
|
|
Bromodomain adjacent to zinc finger domain 1B |
WBSCR10, WBSCR9, WSTF |
Abnormal dermatoglyphic pattern, Abnormal spinal segmentation, Accessory kidney, Aneurysm of aortic arch, Anxiety disorder, Arnold-chiari malformation, Atrial fibrillation, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Bicuspid aortic valve, Bladder diverticulum, Blepharophimosis, Camptodactyly of fingers, Cataract, Cerebral cortical atrophy, Cholelithiasis, Congenital anomaly of neck, Congenital epicanthus, Congenital exomphalos, Congenital hypoplasia of penis, Congenital keratoglobus, Congenital pectus excavatum, Congestive heart failure, Cornea plana, Coronary heart disease, Cryptorchidism, Developmental regression, Diabetes, Diabetes mellitus, Dwarfism, Dysarthria, Dysgraphia, Gastroesophageal reflux disease, Glaucoma, Gout, Gouty arthritis, Hearing loss, Heart failure, Hypercalcemia, Hypertension, Hypertrophic cardiomyopathy, Hyperuricemia, Hypodontia, Hypogonadotropic hypogonadism, Hypothyroidism, Macroglossia, Macrostomia, Macrotia, Malabsorption syndrome, Malignant neoplasm, Mental depression, Mental retardation, Microcephaly, Microdontia, Micrognathism, Migraine, Mitral valve prolapse, Multiple renal cysts, Myocardial infarction, Myopathy, Myopia, Nephrocalcinosis, Nephrolithiasis, Nystagmus-induced head nodding, Obesity, Obsessive-compulsive disorder, Osteopenia, Osteoporosis, Osteosclerosis, Otitis media, Overriding aorta, Patent ductus arteriosus, Pelvic kidney, Peptic ulcer, Peripheral pulmonary artery stenosis, Phakomatosis pigmentovascularis, Polycystic ovary syndrome, Posterior embryotoxon, Precocious puberty, Pulmonary stenosis, Radioulnar synostosis, Rectal prolapse, Renal hypoplasia, Renal insufficiency, Scoliosis, Spina bifida occulta, Strabismus, Stroke, Supravalvar aortic stenosis, Tetralogy of fallot, Ventricular septal defect, Vesicoureteral reflux, Williams syndromeView all (79 more) |
243
|
|
|
Bcl2 modifying factor |
- |
|
244
|
|
|
Basic charge Y-linked 2 |
BPY2A, VCY2, VCY2A |
|
245
|
|
|
BOC cell adhesion associated, oncogene regulated |
Boi, CDON2 |
|
246
|
|
|
BUB3 mitotic checkpoint protein |
BUB3L, hBUB3 |
Ambiguous genitalia, Aortic coarctation, Aortic valve insufficiency, Atrial septal defect, Cafe-au-lait spot, Camptodactyly of fingers, Cataract, Colonic neoplasms, Congenital epicanthus, Dandy-walker syndrome, Developmental delay, Duodenal atresia, Dwarfism, Frontal bossing, Glaucoma, Holoprosencephaly, Hypothyroidism, Intestinal polyposis, Lymphoblastic leukemia, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Mosaic variegated aneuploidy, Multicystic renal dysplasia, Muscular dystrophy, Myelodysplasia, Myelodysplastic syndrome, Nephroblastoma, Rhabdomyosarcoma, Stomach neoplasms, Subaortic stenosis, Vaginal neoplasmsView all (18 more) |
247
|
|
|
Bone morphogenetic protein 15 |
GDF9B, ODG2, POF4 |
46, xx gonadal dysgenesis, 46,xx gonadal dysgenesis, Arachnodactyly, Dwarfism, Gonadal dysgenesis, Gonadal hypoplasia, Hypogonadism, Microcephaly, Osteopenia, Osteoporosis of vertebrae, Sclerocystic ovaries, Ovarian dysgenesis, Ovarian failure, Physiologic amenorrhea, Polycystic ovary syndrome, Premature menopause, Premature ovarian failure, Pulmonary fibrosis, Secondary physiologic amenorrhea, Streak ovary, Uterine anomaliesView all (6 more) |
248
|
|
|
BBSome interacting protein 1 |
BBIP10, BBS18, NCRNA00081, bA348N5.3 |
Bardet-biedl syndrome, Brachydactyly, Cataract, Hypoplasia of the ovary, Congenital hypoplasia of penis, Cryptorchidism, Dwarfism, Hypertension, Hypogonadism, Impaired cognition, Liver fibrosis, Mental retardation, Multicystic renal dysplasia, Nephrotic syndrome, Nystagmus, Obesity, Renal insufficiency, Retinitis pigmentosa, Rod-cone dystrophy, Speech disorders, Syndactyly of fingers, Postaxial hand polydactylyView all (7 more) |
249
|
|
|
BAF chromatin remodeling complex subunit BCL7C |
SMARCJ3 |
|
250
|
|
|
BAF chromatin remodeling complex subunit BCL7B |
SMARCJ2 |
|