|
431
|
|
|
Dynein axonemal heavy chain 11 |
CILD7, DNAHBL, DNAHC11, DNHBL, DPL11 |
Acne, Allergic rhinitis, Asthenozoospermia, Asthma, Breast carcinoma, Bronchiectasis, Bronchitis, Carcinoma, Ciliary dyskinesia, Ciliary dyskinesia, with or without situs inversus, Ciliary dyskinesia, with situs inversus, Ciliopathies, Asplenia, Congenital pectus excavatum, Corneal dystrophy, Coronary heart disease, Dyslexia, Dyslipidemias, Hearing loss, High palate, Hydrocephalus, Lung carcinoma, Lung diseases, Monoclonal gammapathies, Multiple myeloma, Nasal polyposis, Otitis media, Paraproteinemia, Pleural effusion, Pleuritis, Amyloidosis, Rhinitis, Scoliosis, Sinusitis, Situs inversus, Spontaneous pneumothorax, Stomach carcinomaView all (22 more) |
|
432
|
|
|
Delta like non-canonical Notch ligand 1 |
DLK, DLK-1, Delta1, FA1, PREF1, Pref-1, ZOG, pG2 |
|
|
433
|
|
|
Dual specificity tyrosine phosphorylation regulated kinase 4 |
- |
|
|
434
|
|
|
Dolichyl-phosphate mannosyltransferase subunit 1, catalytic |
CDGIE, MPDS |
Antithrombin deficiency, Central visual impairment, Congenital camptodactyly, Congenital disorder of glycosylation, Hemangioma, Microcephaly, Micrognathism, Muscular dystrophy, Nail diseases, Nail dysplasia, Nystagmus, Optic atrophy, Patent ductus arteriosus, Protein c deficiency, Retinal diseases, StrabismusView all (1 more) |
|
435
|
|
|
Dolichyl-phosphate mannosyltransferase subunit 2, regulatory |
CDG1U |
Antithrombin deficiency, Congenital alveolar dysplasia, Cerebellar hypoplasia, Clonic seizures, Congenital contracture, Congenital disorder of glycosylation, Congenital muscular dystrophy with intellectual disability and epilepsy, Developmental delay, Epileptic encephalopathy, High palate, Micrognathism, Myoclonic seizures, Optic atrophy, Osteopenia, Scoliosis, Strabismus, TrigonocephalyView all (2 more) |
|
436
|
|
|
Deleted in lymphocytic leukemia 2 |
ALT1, BCMSUN, DLB2, LEU2, LINC00022, MIR15AHG, NCRNA00022, RFP2, RFP2OS, TRIM13OS |
|
|
437
|
|
|
DEAD-box helicase 18 |
Has1, MrDb |
|
|
438
|
|
|
Dynein 2 intermediate chain 2 |
CFAP133, DIC5, FAP133, SRTD11, WDR34, bA216B9.3 |
Agenesis of corpus callosum, Ambiguous genitalia, Asphyxiating thoracic dystrophy, Brachydactyly, Cataract, Cerebellar hypoplasia, Congenital duplication of uterus, Congenital epicanthus, Congenital hepatic fibrosis, Pulmonary hypoplasia, Congenital hypoplasia of penis, Congenital omphalocele, Cryptorchidism, Dandy-walker syndrome, Dwarfism, Ectopic anus, Esophageal atresia, Foot polydactyly, Frontal bossing, Hydronephrosis, Hydrops fetalis, Imperforate anus, Jeune syndrome, Jeune thoracic dystrophy, Kidney disease, Macrocephaly, Majewski syndrome, Micrognathism, Micromelia, Nephronophthisis, Osteochondrodysplasia, Polydactyly, Renal cyst, Renal hypoplasia, Renal insufficiency, Short rib-polydactyly syndrome, Short-rib thoracic dysplasia with or without polydactyly, Skeletal dysplasia, Syndactyly of the toes, Thoracic dysplasia, Postaxial hand polydactylyView all (26 more) |
|
439
|
|
|
Docking protein 2 |
p56DOK, p56dok-2 |
|
|
440
|
|
|
DIRAS family GTPase 3 |
ARHI, NOEY2 |
|
