|
201
|
|
|
Barttin CLCNK type accessory subunit beta |
BART, DFNB73 |
Allergic rhinitis, Bartter syndrome, Bartter syndrome with sensorineural deafness, Hearing loss, Hydrops fetalis, Hyperaldosteronism, Hypernatriuria, Hypochloremia, Hypokalemia, Mental retardation, Motor delay, Non-syndromic sensorineural deafness, Renal insufficiency, Sensorineural deafness with mild renal dysfunction |
|
202
|
|
|
BTG anti-proliferation factor 2 |
APRO1, PC3, TIS21 |
|
|
203
|
|
|
Bromodomain and PHD finger containing 1 |
BR140, IDDDFP |
Blepharophimosis, Congenital camptodactyly, Congenital clubfoot, Developmental delay, Dysmorphic features, Intellectual developmental disorder with dysmorphic facies and ptosis, Macrostomia, Mental retardation, Microstomia, Neurodevelopmental disorders, Prostatic neoplasms, Prostate cancer, Ptosis, Strabismus |
|
204
|
|
|
BAG cochaperone 6 |
BAG-6, BAT3, D6S52E, G3 |
|
|
205
|
|
|
BRCA1/BRCA2-containing complex subunit 3 |
BRCC36, C6.1A, CXorf53 |
|
|
206
|
|
|
Basic helix-loop-helix family member e41 |
BHLHB3, DEC2, FNSS1, SHARP1, hDEC2 |
|
|
207
|
|
|
BCL2 like 14 |
BCLG |
|
|
208
|
|
|
Baculoviral IAP repeat containing 7 |
KIAP, LIVIN, ML-IAP, MLIAP, RNF50 |
|
|
209
|
|
|
BEN domain containing 5 |
C1orf165 |
|
|
210
|
|
|
Bardet-Biedl syndrome 10 |
C12orf58 |
Asphyxiating thoracic dystrophy, Bardet-biedl syndrome, Ciliopathies, Hypoplasia of the ovary, Congenital hypoplasia of penis, Cryptorchidism, Disorder of eye, Dwarfism, Foot polydactyly, Hearing loss, Hypertension, Hypogonadism, Impaired cognition, Liver fibrosis, Macular degeneration, Mental retardation, Multicystic renal dysplasia, Multiple congenital anomalies, Nephrotic syndrome, Nyctalopia, Nystagmus, Obesity, Polycystic kidney disease, Polydactyly, Polydactyly of toes, Renal cyst, Renal insufficiency, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophy, Speech disorders, Syndactyly of fingers, Postaxial hand polydactylyView all (18 more) |
