341
|
|
|
DnaJ heat shock protein family (Hsp40) member C3 |
ACPHD, ERdj6, HP58, P58, P58IPK, PRKRI, p58(IPK) |
Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus, Atrophy of the spinal cord, Brainstem atrophy, Cerebellar atrophy, Cerebral atrophy, Demyelinating neuropathy, Diabetes mellitus, Diabetes mellitus-central and peripheral neurodegeneration syndrome, Dwarfism, Hearing loss, Mental retardation, Nervous system diseases, Prostatic neoplasms, Prostate cancer, Sensorimotor neuropathy, Sensorineural hearing lossView all (1 more) |
342
|
|
|
Dynein axonemal heavy chain 7 |
CILD50 |
|
343
|
|
|
DnaJ heat shock protein family (Hsp40) member C12 |
HPANBH4, JDP1 |
|
344
|
|
|
Diablo IAP-binding mitochondrial protein |
DFNA64, SMAC |
|
345
|
|
|
Dual specificity phosphatase 22 |
JKAP, JSP-1, JSP1, LMW-DSP2, LMWDSP2, MKP-x, MKPX, VHX |
|
346
|
|
|
Deleted in azoospermia 3 |
pDP1679 |
|
347
|
|
|
Deleted in azoospermia 2 |
pDP1678 |
|
348
|
|
|
Deleted in azoospermia 4 |
pDP1680, pDP1681 |
|
349
|
|
|
DS cell adhesion molecule like 1 |
DSCAM2 |
|
350
|
|
|
Dedicator of cytokinesis 6 |
AOS2, ZIR1 |
Acquired porencephaly, Adams-oliver syndrome, Alopecia, Aplasia cutis congenita, Brachydactyly, Cataract, Cirrhosis, Congenital arteriovenous malformation, Congenital atresia of pulmonary artery, Congenital cerebral hernia, Congenital hepatic fibrosis, Cutis marmorata, Developmental delay, Dysmorphic features, Esophageal varix, Hydrocephalus, Leukopenia, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Periventricular leukomalacia, Porencephalic cyst, Portal hypertension, Pulmonary arterial hypertension, Rheumatic aortic stenosis, Strabismus, Syndactyly of fingers, Talipes, Tetralogy of fallotView all (15 more) |