pachyonychia congenita (Q3360152)

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rare group of autosomal dominant skin disorders that are caused by a mutation in one of five different keratin genes
  • Jackson-Lawler type pachyonychia congenita
  • Jadassohn-Lewandowsky syndrome
  • Pachyonychia congenita, Jadassohn-Lewandowky type
  • Pachyonychia congenita type 1
  • congenital pachyonychia
  • Jackson-Lawler syndrome
  • Pachyonychia congenita syndrome
  • PC
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Language Label Description Also known as
English
pachyonychia congenita
rare group of autosomal dominant skin disorders that are caused by a mutation in one of five different keratin genes
  • Jackson-Lawler type pachyonychia congenita
  • Jadassohn-Lewandowsky syndrome
  • Pachyonychia congenita, Jadassohn-Lewandowky type
  • Pachyonychia congenita type 1
  • congenital pachyonychia
  • Jackson-Lawler syndrome
  • Pachyonychia congenita syndrome
  • PC

Statements

Identifiers

Pachyonychia congenita
Congenital pachyonychia
Jackson-Lawler syndrome
Jadassohn-Lewandowsky syndrome
Pachyonychia congenita syndrome
PC
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