|
161
|
|
|
BLM RecQ like helicase |
BS, MGRISCE1, RECQ2, RECQL2, RECQL3 |
Azoospermia, Bloom syndrome, Bronchiectasis, Camptodactyly of fingers, Hereditary cancer syndrome, Carcinoma, Cryptorchidism, Diabetes mellitus, Dolichocephaly, Dwarfism, Gastrointestinal neoplasms, Hypertrichosis, Ichthyosis, Immunologic deficiency syndromes, Leukemia, Lung diseases, Lymphocytic leukemia, Lymphoma, Lymphoblastic leukemia, Malignant neoplasm, Mental retardation, Microcephaly, Miller dieker syndrome, Monocytic leukemia, Myelodysplastic syndrome, Sinusitis, Specific learning disorder, Syndactyly, Syndactyly of fingersView all (14 more) |
|
162
|
|
|
Bleomycin hydrolase |
BH, BMH |
|
|
163
|
|
|
Biliverdin reductase A |
BLVR, BVR, BVRA, BVRalpha |
|
|
164
|
|
|
BCR pseudogene 1 |
BCR-1 |
|
|
165
|
|
|
Biliverdin reductase B |
BVRB, FLR, HEL-S-10, SDR43U1 |
|
|
166
|
|
|
Basonuclin zinc finger protein 1 |
BNC, BSN1, HsT19447, POF16, bn1 |
|
|
167
|
|
|
BMI1 proto-oncogene, polycomb ring finger |
FLVI2/BMI1, PCGF4, RNF51, flvi-2/bmi-1 |
|
|
168
|
|
|
Bone morphogenetic protein 1 |
OI13, PCOLC, PCP, PCP2, TLD |
|
|
169
|
|
|
BCL11 transcription factor B |
ATL1, ATL1-alpha, ATL1-beta, ATL1-delta, ATL1-gamma, CTIP-2, CTIP2, IDDFSTA, IMD49, RIT1, SMARCM2, ZNF856B, hRIT1-alpha |
Agenesis of corpus callosum, Anxiety disorder, Bipolar disorder, Colorectal cancer, Congenital epicanthus, Congenital exomphalos, Cutis laxa, Dermatitis, Developmental delay, Dysmorphic features, Eosinophilia, Hyperopia, Hypodontia, Immunodeficiency, Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities, Lymphoma, Lymphoblastic leukemia, Lymphopenia, Mental retardation, Microdontia, Micrognathism, Microstomia, Multiple congenital anomalies, Myopia, Oligodontia, Posteriorly rotated ear, Schizophrenia, Severe combined immunodeficiency disease, Spastic quadriplegiaView all (14 more) |
|
170
|
|
|
Bone morphogenetic protein 2 |
BDA2, BMP2A, SSFSC, SSFSC1 |
20p12.3 microdeletion syndrome, Acrocephaly, Alopecia, Arthropathy, Atrial septal defect, Azoospermia, Bone disease, Brachycephaly, Brachydactyly, Breast cancer, Mammary neoplasms, Breast carcinoma, Camptodactyly of fingers, Cardiomyopathy, Cirrhosis, Colorectal cancer, Colorectal neoplasms, Congenital epicanthus, Congenital pectus carinatum, Congenital pectus excavatum, Congestive heart failure, Craniosynostosis, Developmental delay, Diabetes mellitus, Dwarfism, Erectile dysfunction, Gastric cancer, Hearing loss, Hemochromatosis, Hereditary hemochromatosis, High palate, Hypogonadotropic hypogonadism, Hypoplasia of the maxilla, Isolated right ventricular hypoplasia, Liver carcinoma, Macrocephaly, Marfan syndrome, Metopic synostosis, Microstomia, Microtia, Myopia, Osteoporosis, Paroxysmal supraventricular tachycardia, Pierre-robin syndrome, Pleural effusion, Posteriorly rotated ear, Pulmonary stenosis, Scaphocephaly, Short stature, facial dysmorphism and skeletal anomalies with or without cardiac anomalies, Sleep apnea, Spina bifida occulta, Spondylolisthesis, Stomach neoplasms, Syndactyly of the toes, Synophrys, Synostotic anterior plagiocephaly, Synostotic posterior plagiocephaly, Testicular atrophy, Transposition of great vessels, Trigonocephaly, Uremia, Vascular diseases, Ventricular septal defect, Wolff-parkinson-white syndromeView all (49 more) |
