eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | hutchinson-gilford progeria syndrome |
| Comorbidity | C0040188|tic disorders |
| Sentences | 1 |
| PubMedID- 24637396 | Mutations in the lamin a gene (lmna) cause severe genetic disorders, one of which is hutchinson-gilford progeria syndrome (hgps), a disease triggered by a dominant mutant named progerin. |
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