eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | hutchinson-gilford progeria syndrome |
| Comorbidity | C0043119|werner syndrome |
| Sentences | 1 |
| PubMedID- 24620826 | werner syndrome is one of the genetic progeria disorders with autosomal recessive inheritance, and it is caused by mutations of the werner syndrome (wrn) gene[1-3]. |
Page: 1