|
51
|
|
|
Bromodomain PHD finger transcription factor |
FAC1, FALZ, NEDDFL, NURF301 |
17q24.2 microdeletion syndrome, Cubitus valgus, Anxiety disorder, Autism, Urinary bladder cancer, Bladder neoplasm, Camptodactyly of fingers, Cataract, Choanal atresia, Clinodactyly, Congenital epicanthus, Cryptorchidism, Developmental delay, Dwarfism, Dysmorphic features, Endometrial carcinoma, Exocrine pancreatic insufficiency, Exotropia, Expressive language delay, Fifth finger distal phalanx clinodactyly, Grammar-specific speech disorder, Hallucinations, High palate, Isolated somatotropin deficiency, Lung carcinoma, Lung adenocarcinoma, Mental retardation, Microcephaly, Micrognathism, Microstomia, Microtia, Mood swings, Multiple congenital anomalies, Myopia, Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies, Otitis media, Otosclerosis, Patent ductus arteriosus, Persistent pupillary membranes, Psoriasis, Ptosis, Pulmonary stenosis, Scoliosis, Secondary physiologic amenorrhea, Strabismus, Syndromic mental retardation, Synophrys, Vesicoureteral refluxView all (33 more) |
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52
|
|
|
BRCA1 associated ATM activator 1 |
BAAT1, C7orf27, NEDCAS, RMFSL |
Camptodactyly of fingers, Cerebellar atrophy, Congenital epicanthus, Developmental delay, Dysautonomia, Dysmorphic features, High palate, Hypoplasia of corpus callosum, Lethal spasticity-epileptic encephalopathy syndrome, Mental retardation, Microcephaly, Myoclonic seizures, Neurodevelopmental disorder with cerebellar atrophy and with or without seizures, Nystagmus, Rigidity and multifocal seizure syndrome |
|
53
|
|
|
BEN domain containing 7 |
C10orf30 |
|
|
54
|
|
|
BOP1 ribosomal biogenesis factor |
- |
|
|
55
|
|
|
BICD cargo adaptor 2 |
SMALED2, SMALED2A, SMALED2B, bA526D8.1 |
Arthrogryposis multiplex congenita, Cerebellar hypoplasia, Cerebral cortical atrophy, Congenital clubfoot, Developmental dysplasia of the hip, Congenital foot contraction deformities, Distal lower limb amyotrophy, Hydrocephalus, Hydrops fetalis, Hypoplasia of corpus callosum, Macrocephaly, Mental retardation, Micrognathism, Motor delay, Pachygyria, Pterygium, Respiratory failure, Scoliosis, Spinal muscular atrophy, Spinal muscular atrophy, lower extremity-predominant, Vertical talusView all (6 more) |
|
56
|
|
|
Bromodomain containing 4 |
CAP, CDLS6, FSHRG4, HUNK1, HUNKI, MCAP |
Alopecia, Alopecia, male pattern, Androgenetic alopecia, Carcinoma, Colonic neoplasms, Congenital heart defects, Congenital muscular hypertrophy-cerebral syndrome, Cornelia de lange syndrome, Ewing sarcoma, Giant cell glioblastoma, Glioblastoma, Leukemia, Medulloblastoma, Medullomyoblastoma, Mental retardation, Microcephaly, Neuroblastoma, Osteosarcoma, Pancreatic carcinoma, Pancreatoblastoma, Polycystic kidney disease, Prostatic neoplasms, Prostate cancer, Pseudopelade, Oropharyngeal carcinoma, Thyroid neoplasm, Thyroid carcinoma, Thyroid gland follicular adenomaView all (13 more) |
|
57
|
|
|
Beta-secretase 1 |
ASP2, BACE, HSPC104 |
|
|
58
|
|
|
Bromodomain containing 1 |
BRL, BRPF1, BRPF2 |
|
|
59
|
|
|
BCL2 like 13 |
BCL-RAMBO, Bcl2-L-13, MIL1 |
|
|
60
|
|
|
Bromodomain and WD repeat domain containing 3 |
BRODL, DCAF20, MRX93, XLID93 |
|
