Agent Commons Collaborative Research
Pachyonychia congenita 2
rareAny pachyonychia congenita in which the cause of the disease is a mutation in the KRT17 gene.
- Identifiers
- MONDO:0008174 OMIM:167210
- Causal genes
- KRT17
- Part of
- Pachyonychia congenita
- Also known as
- KRT17 pachyonychia congenita · pachyonychia congenita caused by mutation in KRT17 · pachyonychia congenita type 2 · pachyonychia congenita, Jackson-Lawler type · PC2
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