|
191
|
|
|
Basigin (Ok blood group) |
5F7, CD147, EMMPRIN, EMPRIN, HAb18G, OK, TCSF |
|
|
192
|
|
|
Bone marrow stromal cell antigen 1 |
CD157, cADPR2 |
|
|
193
|
|
|
Betacellulin |
- |
|
|
194
|
|
|
Biotinidase |
- |
Alopecia, Autism, Biotinidase deficiency, Conjunctivitis, Coronary heart disease, Coronary syndrome, Developmental delay, Diverticular diseases, Dysmorphic features, Hearing loss, Keratoconjunctivitis, Laryngospasm, Myoclonic seizures, Myopia, Optic atrophy, Perioral eczema, Psoriasis, Seborrheic dermatitisView all (3 more) |
|
195
|
|
|
BTG anti-proliferation factor 1 |
APRO2 |
|
|
196
|
|
|
Bruton tyrosine kinase |
AGMX1, AT, ATK, BPK, IGHD3, IMD1, PSCTK1, XLA |
Agammaglobulinemia, Agammaglobulinemia with growth hormone deficiency, x-linked, Agammaglobulinemia, x-linked, Alopecia, Anemia, Arthritis, Breast adenocarcinoma, Breast cancer, Mammary neoplasms, Breast carcinoma, Conjunctivitis, Cor pulmonale, Dwarfism, Encephalitis, Epididymitis, Glossoptosis, Hearing loss, Hypogammaglobulinemia, Immunologic deficiency syndromes, Isolated somatotropin deficiency, Lymphocytic leukemia, Lung carcinoma, Malabsorption syndrome, Neoplasms, Neutropenia, Osteomyelitis, Otitis media, Prostatitis, Pyoderma, Sinusitis, Somatotropin deficiencyView all (16 more) |
|
197
|
|
|
BUB1 mitotic checkpoint serine/threonine kinase |
BUB1A, BUB1L, MCPH30, hBUB1 |
Ambiguous genitalia, Aortic coarctation, Aortic valve insufficiency, Atrial septal defect, Cafe-au-lait spot, Camptodactyly of fingers, Cataract, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Congenital epicanthus, Dandy-walker syndrome, Developmental delay, Duodenal atresia, Dwarfism, Frontal bossing, Glaucoma, Hereditary nonpolyposis colorectal cancer, Holoprosencephaly, Hypothyroidism, Intestinal polyposis, Leiomyosarcoma of uterus, Liver carcinoma, Lymphoblastic leukemia, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Mosaic variegated aneuploidy, Multicystic renal dysplasia, Muscular dystrophy, Myelodysplasia, Myelodysplastic syndrome, Nephroblastoma, Pancreatic cancer, Renal carcinoma, Rhabdomyosarcoma, Stomach neoplasms, Subaortic stenosis, Bladder carcinoma, Vaginal neoplasmsView all (26 more) |
|
198
|
|
|
BUB1 mitotic checkpoint serine/threonine kinase B |
BUB1beta, BUBR1, Bub1A, MAD3L, MVA1, SSK1, hBUBR1 |
Agenesis of corpus callosum, Ambiguous genitalia, Aortic coarctation, Aortic valve insufficiency, Atrial septal defect, Brachycephaly, Cafe-au-lait spot, Camptodactyly of fingers, Neoplasm, Cataract, Cerebellar hypoplasia, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Congenital epicanthus, Congenital microcephaly, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Duodenal atresia, Dwarfism, Embryonal neoplasm, Embryonal rhabdomyosarcoma, Esophagus neoplasm, Frontal bossing, Tumor, Glaucoma, Hereditary nonpolyposis colorectal cancer, Holoprosencephaly, Hydrocephalus, Hypospadias, Hypothyroidism, Intestinal polyposis, Leiomyosarcoma of uterus, Leukemia, Liver carcinoma, Lymphoblastic leukemia, Mental retardation, Microcephaly, Micrognathism, Microlissencephaly, Microphthalmos, Mosaic variegated aneuploidy, Multicystic renal dysplasia, Muscular dystrophy, Myelodysplasia, Myelodysplastic syndrome, Myoclonic seizures, Nephroblastoma, Nystagmus, Ovarian neoplasm, Penis agenesis, Posteriorly rotated ear, Renal carcinoma, Renal cyst, Rhabdomyosarcoma, Seizure, Severe combined immunodeficiency disease, Stomach neoplasms, Subaortic stenosis, Bladder carcinoma, Vaginal neoplasmsView all (47 more) |
|
199
|
|
|
Basic helix-loop-helix family member a9 |
BHLHF42, CCSPD |
Brachydactyly, Camptodactyly of fingers, Camptosynpolydactyly, Congenital camptodactyly, Short femur, Congenital omphalocele, Ectrodactyly, Gollop-wolfgang complex, Hypoplasia of thumb, Polydactyly, Split-hand-foot malformation with sensorineural hearing loss, Split-hand-foot malformation with long bone deficiency, Syndactyly, mesoaxial synostotic, with phalangeal reduction, Syndactyly of fingers, Syndactyly of the toes, Tibial aplasia-ectrodactyly syndrome, Postaxial hand polydactylyView all (2 more) |
|
200
|
|
|
Bestrophin 1 |
ARB, BEST, BMD, Best1V1Delta2, RP50, TU15B, VMD2 |
Bestrophinopathy, Cataract, Choroideremia, Congenital hypoplasia of penis, Cystoid macular retinal degeneration, Diabetes mellitus, Disorder of eye, Foveomacular vitelliform dystrophy, Glaucoma, Hearing loss, Hyperinsulinism, Hyperopia, Hypogonadism, Keratoconus, Age-related macular degeneration, Macular dystrophy, Mental retardation, Microcornea, Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma, Microphthalmos, Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome, Nanophthalmos, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinal detachment, Retinal dystrophy, Retinal nonattachment, Retinitis pigmentosa, Rod-cone dystrophy, Scleral staphyloma, Staphyloma posticum, Stargardt disease, Strabismus, Vitelliform macular dystrophy, VitreoretinochoroidopathyView all (22 more) |
