| Disease ID | Source | Name | Description |
| 107600 | OMIM | Aplasia cutis congenita, non-syndromic (ACC) | A disorder characterized by congenital absence of a portion of skin in a localized or widespread area of the body. The lesions are most commonly localized on the scalp, however aplasia cutis congenita can affect any part of the body. The disease is caused by variants affecting the gene represented in this entry. |