Pachyonychia congenita 2

Any pachyonychia congenita in which the cause of the disease is a mutation in the KRT17 gene.

Also known as: KRT17 pachyonychia congenita, pachyonychia congenita 2, pachyonychia congenita caused by mutation in KRT17, pachyonychia congenita type 2, PC2, pachyonychia congenita, Jackson-Lawler type, pachyonychia congenita, Jackson-Lawler type, formerly

7 clinical trials for this condition and its sub-types.