|
401
|
|
|
Dedicator of cytokinesis 8 |
HEL-205, HIES2, MRD2, ZIR8 |
Anal canal carcinoma, Asthma, Carcinoma, Carcinoma of vulva, Cerebral angiitis, Dermatitis, Development disorder, Eczema, Eosinophilia, Hyper-immunoglobulin e syndrome, Mental retardation, Lung diseases, Lymphoma, Malignant melanoma of skin, Melanoma, Neoplasms, Neuroblastoma, Neurodevelopmental disorders, Non-syndromic intellectual disability, Otitis media, Severe combined immunodeficiency disease, Sinusitis, Stat3 deficiency, Subarachnoid hemorrhageView all (9 more) |
|
402
|
|
|
DiGeorge syndrome critical region gene 6 |
- |
Blepharophimosis, Conotruncal anomaly face syndrome, Digeorge syndrome, Dwarfism, Mental retardation, Microcephaly, Mood swings, Paranoia, Pierre-robin syndrome, Posterior embryotoxon, Proline dehydrogenase deficiency, Pulmonary dysgenesis, Schizophrenia, Shprintzen syndrome, Specific learning disorder, Velopharyngeal insufficiency, Ventricular septal defectView all (2 more) |
|
403
|
|
|
Dysferlin |
FER1L1, LGMD2B, LGMDR2, MMD1 |
Amyotrophy, Arthritis, Brachial plexus neuropathy, Breast cancer, Bundle branch block, Congenital myopathy, Distal amyotrophy, Distal myopathy with anterior tibial onset, Distal upper limb amyotrophy, Dysferlinopathy, Dysphagia, Juvenile arthritis, Limb-girdle muscular dystrophy, Miyoshi muscular dystrophy, Miyoshi myopathy, Muscular dystrophy, Myopathy, Peroneal muscle atrophy, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Spinal muscular atrophy, Still disease, Ventricular hypertrophyView all (8 more) |
|
404
|
|
|
Dynein regulatory complex subunit 3 |
CFAP134, LRRC48 |
|
|
405
|
|
|
DEAD-box helicase 59 |
OFD5, ZNHIT5 |
Agenesis of corpus callosum, Breast cancer, Cleft soft palate, Dental enamel hypoplasia, Ectopic accessory finger-like appendage, Foot polydactyly, Frontal bossing, Hirschsprung disease, Hypodontia, Mental retardation, Microcephaly, Orofaciodigital syndrome, Polydactyly, Scoliosis, Tetralogy of fallot, Postaxial hand polydactylyView all (1 more) |
|
406
|
|
|
Dynein axonemal light chain 1 |
C14orf168, CILD16, LC1 |
Asthenozoospermia, Asthma, Bronchiectasis, Ciliary dyskinesia, Asplenia, Congenital pectus excavatum, Corneal dystrophy, Bronchitis, Hearing loss, Hydrocephalus, Lung diseases, Nasal polyposis, Otitis media, Rhinitis, Scoliosis, Sinusitis, Situs inversusView all (2 more) |
|
407
|
|
|
Dystrobrevin binding protein 1 |
BLOC1S8, DBND, HPS7, My031, SDY |
Albinism, Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells, Behavior disorders, Bipolar disorder, Carcinoma, Hermansky-pudlak syndrome, Mental disorders, Mental depression, Mental depression with psychotic features, Mood disorder, Nystagmus, Ocular albinism, Schizophrenia |
|
408
|
|
|
Defective in cullin neddylation 1 domain containing 5 |
DCNL5, SCCRO5 |
|
|
409
|
|
|
DOT1 like histone lysine methyltransferase |
DOT1, KMT4, NDNS |
|
|
410
|
|
|
Dual specificity tyrosine phosphorylation regulated kinase 2 |
- |
|
