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disease > genetic disease > hereditary disease > Jackson-Lawler pachyonychia
disease > congenital disease > malformation > ectodermal dysplasia > Jackson-Lawler pachyonychia
disease > stomatology > dental disease > ectodermal dysplasia > Jackson-Lawler pachyonychia
disease > dysplasia > ectodermal dysplasia > Jackson-Lawler pachyonychia
disease > genetic disease > hereditary disease > ectodermal dysplasia > Jackson-Lawler pachyonychia
... > disease > skin appendages disease > skin disease > sweat gland disease > ectodermal dysplasia > Jackson-Lawler pachyonychia
disease > skin appendages disease > hypotrichosis > ectodermal dysplasia > Jackson-Lawler pachyonychia
disease > skin appendages disease > nail disease > Jackson-Lawler pachyonychia
disease > skin appendages disease > skin disease > dyskeratosis > Jackson-Lawler pachyonychia

Preferred term

Jackson-Lawler pachyonychia  

Definition(s)

  • Pachyonychia congenita type II (also known as "Jackson–Lawler pachyonychia congenita" and "Jackson–Sertoli syndrome") is an autosomal dominant keratoderma presenting with a limited focal plantar keratoderma that may be very minor, with nails changes that may be evident at birth, but more commonly develop within the first few months of life. (Wikipedia)

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URI

http://data.loterre.fr/ark:/67375/VH8-DVC9HSRR-7

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