eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | pachyonychia congenita |
| Symptom | C0259771|steatocystoma multiplex |
| Sentences | 1 |
| PubMedID- 24842198 | Familial pachyonychia congenita with steatocystoma multiplex and multiple abscesses of the scalp due to the p.asn92ser mutation in keratin 17. |
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