|
291
|
|
|
DENN domain containing 6B |
AFI1B, FAM116B |
|
|
292
|
|
|
DnaJ heat shock protein family (Hsp40) member B9 |
ERdj4, MDG-1, MDG1, MST049, MSTP049 |
|
|
293
|
|
|
DPY19L2 pseudogene 3 |
- |
|
|
294
|
|
|
- |
- |
|
|
295
|
|
|
Developmentally regulated GTP binding protein 1 |
NEDD3, TANALS |
|
|
296
|
|
|
Discoidin domain receptor tyrosine kinase 2 |
MIG20a, NTRKR3, TKT, TYRO10, WRCN |
Atlantoaxial abnormality, Calcification of falx cerebri, Calcification of trachea, Carcinoma, Choroidal melanoma, Congenital anomaly of neck, Congenital pectus excavatum, Developmental delay, Dupuytren contracture, Elbow flexion contracture, Frontal bossing, High palate, Lung carcinoma, Lung adenocarcinoma, Micrognathism, Micromelia, Osteolysis involving bones of the feet, Proptosis, Scoliosis, Spinal cord compression, Spondyloepimetaphyseal dysplasia, Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome, Spondylometaphyseal dysplasia, Syringomyelia, Thoracic hypoplasiaView all (10 more) |
|
297
|
|
|
Double homeobox A |
- |
|
|
298
|
|
|
Dual oxidase 2 |
LNOX2, NOXEF2, P138-TOX, TDH6, THOX2 |
Congenital exomphalos, Congenital hypothyroidism, Congenital myxedema, Developmental delay, Dwarfism, Dysmorphic features, Endemic cretinism, Genetic transient congenital hypothyroidism, Hypersomnia, Hypothyroidism, Macroglossia, Mental retardation, Thyroid dyshormonogenesis, Transient hypothyroxinaemia of prematurity |
|
299
|
|
|
Deleted in esophageal cancer 1 |
CTS9, DEC1 |
Ankylosing spondylitis, Cardiovascular diseases, Cholangitis, Cholecystolithiasis, Cholelithiasis, Chronic obstructive pulmonary disease, Crohn disease, Deafness, Inflammatory bowel disease, Leprosy, Mental depression, Mood disorder, Osteoarthritis of hip, Biliary cirrhosis, Psoriasis, Sleep disorders, Ulcerative colitisView all (2 more) |
|
300
|
|
|
DEF6 guanine nucleotide exchange factor |
IBP, IMD87, SLAT, SWAP70L |
|
