111
|
|
|
Defensin alpha 3 |
DEF3, HNP-3, HNP3, HP-3, HP3 |
|
112
|
|
|
Defensin alpha 4 |
DEF4, HNP-4, HP-4, HP4 |
|
113
|
|
|
Defensin alpha 5 |
DEF5, HD-5 |
|
114
|
|
|
Defensin alpha 6 |
DEF6, HD-6 |
|
115
|
|
|
Defensin beta 1 |
BD1, DEFB-1, DEFB101, HBD1 |
|
116
|
|
|
Desmin |
CDCD3, CSM1, CSM2, LGMD1D, LGMD1E, LGMD2R |
Anaplastic carcinoma, Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Atrioventricular block, Breast cancer, Mammary neoplasms, Breast carcinoma, Bright disease, Bulbar palsy, Carcinoma, Cardiomyopathy, Charcot-marie-tooth disease, Concentric hypertrophic cardiomyopathy, Congenital clubfoot, Congenital diaphragmatic hernia, Posterolateral diaphragmatic hernia, Morgagni diaphragmatic hernia, Congestive heart failure, Desminopathy, Dilated cardiomyopathy, Facial paralysis, Gastric cancer, Glomerulonephritis, Hearing loss, Hyperhomocysteinemia, Left bundle-branch block, Limb-girdle muscular dystrophy, Lipoatrophy, Lipodystrophy, Marfan syndrome, Myofibrillar myopathy, Myopathy, Nephrosis, Neurogenic scapuloperoneal syndrome, Neuromuscular diseases, Palmoplantar keratoderma, Paroxysmal atrial fibrillation, Paroxysmal supraventricular tachycardia, Peroneal muscle atrophy, Stark-kaeser syndrome, Stomach neoplasms, Transitional atrioventricular canal defectView all (27 more) |
117
|
|
|
DNA fragmentation factor subunit alpha |
DFF-45, DFF1, ICAD |
|
118
|
|
|
Dishevelled binding antagonist of beta catenin 2 |
C6orf116, DAPPER2, DPR2, bA503C24.7 |
|
119
|
|
|
DiGeorge syndrome chromosome region |
CATCH22, DGS, VCF |
|
120
|
|
|
Deoxyguanosine kinase |
MTDPS3, NCPH, NCPH1, PEOB4, dGK |
Cataract, Cerebral atrophy, Cerebral cortical atrophy, Cholestasis, Cruveilhier-baumgarten syndrome, Dementia, Deoxyguanosine kinase deficiency, Dysphagia, Epileptic encephalopathy, Fatty liver, Hearing loss, Hyperbilirubinemia, Hypoalbuminemia, Hypoglycemia, Impaired cognition, Limb-girdle muscle atrophy, Liver failure, Mental depression, Microcephaly, Micronodular cirrhosis, Mitochondrial dna depletion syndrome, hepatocerebral, Mitochondrial dna depletion syndrome, Mitochondrial myopathy, Multiple mitochondrial dna deletion syndrome, Nystagmus, Optic atrophy, Peripheral axonal neuropathy, Polyneuropathy, Portal hypertension, Progressive external ophthalmoplegia, Progressive external ophthalmoplegia with mitochondrial dna deletions, Ptosis, StrabismusView all (18 more) |