|
511
|
|
|
Retina and anterior neural fold homeobox 2 |
ARMD6, CORD11, QRX, RAXL1, RP95 |
|
|
512
|
|
|
Ribosomal oxygenase 2 |
JMJD10, MDIG, MINA, MINA53, NO52, ROX |
|
|
513
|
|
|
R-spondin 3 |
CRISTIN1, PWTSR, THSD2 |
|
|
514
|
|
|
Regulator of G protein signaling 5 |
MST092, MST106, MST129, MSTP032, MSTP092, MSTP106, MSTP129 |
|
|
515
|
|
|
RELT TNF receptor |
AI3C, TNFRSF19L, TRLT |
|
|
516
|
|
|
RNA binding motif protein 17 |
SPF45 |
|
|
517
|
|
|
RALBP1 associated Eps domain containing 1 |
NBIA7, RALBP1 |
|
|
518
|
|
|
Rhophilin Rho GTPase binding protein 2 |
P76RBE, RHOBP |
|
|
519
|
|
|
RUNX family transcription factor 2 |
AML3, CBF-alpha-1, CBFA1, CCD, CCD1, CLCD, OSF-2, OSF2, PEA2aA, PEBP2aA |
Arthritis, Brachycephaly, Brachydactyly, Congenital alveolar dysplasia, Camptodactyly of fingers, Cleidocranial dysplasia, Cleidocranial dysplasia, forme fruste, dental anomalies only, Cleidocranial dysplasia, forme fruste, with brachydactyly, Short clavicles, Craniosynostosis, Defect of skull ossification, Dental enamel hypoplasia, Dwarfism, Frontal bossing, Glossoptosis, Hypoplasia of the maxilla, Macrocephaly, Malocclusion, Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly, Metaphyseal dysplasia with maxillary hypoplasia, with or without brachydactyly, Metaphyseal dysplasia-maxillary hypoplasia-brachydactly syndrome, Micrognathism, Odontome, Osteoarthritis of hip, Osteoarthrosis deformans, Osteochondrodysplasia, Osteoporosis, Osteoporosis of vertebrae, Osteosarcoma, Osteosclerosis, Otitis media, Progressive supranuclear palsy, Psoriatic arthritis, Pyle metaphyseal dysplasia, Rheumatoid arthritis, Scoliosis, Sinusitis, Skeletal dysplasia, Sleep apnea, Spina bifida occulta, Spondyloarthritis, Spondylolisthesis, Spondylolysis, Stomatognathic system abnormalities, Syringomyelia, UremiaView all (31 more) |
|
520
|
|
|
RuvB like AAA ATPase 1 |
ECP-54, ECP54, INO80H, NMP 238, NMP238, PONTIN, Pontin52, RVB1, TIH1, TIP49, TIP49A |
|
