PedAM
Pediatric Disease Annotations & Medicines
| Disease | arteriosclerosis |
| Phenotype | C0086543|cataracts |
| Sentences | 1 |
| PubMedID- 23050038 | Patients with the rare autosomal recessive disorder werner syndrome, in which the wrn gene is mutated, display genomic instability and telomere shortening on the cellular and premature aging on the organismic level with symptoms resembling normal human aging in many aspects including cataracts, graying of hair and alopecia, atherosclerosis, osteoporosis, and higher cancer incidence. |
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