Pachyonychia Congenita
A group of inherited ectodermal dysplasias whose most prominent clinical feature is hypertrophic nail dystrophy resulting in PACHYONYCHIA. Several specific subtypes of pachyonychia congenita have been associated with mutations in genes that encode KERATINS.
Year introduced: 2007
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Tree Number(s): C16.131.077.350.856, C16.131.831.350.856, C16.320.850.250.856, C17.800.529.594, C17.800.804.350.856, C17.800.827.250.856
MeSH Unique ID: D053549
Entry Terms:
- Congenital Pachyonychia
- Pachyonychia, Congenital
- Pachyonychia Congenita Syndrome
- Pachyonychia Congenita, Type 1
- Pachyonychia Congenita, Jadassohn-Lewandowsky Type
- Pachyonychia Congenita, Jadassohn Lewandowsky Type
- Jadassohn-Lewandowsky Syndrome
- Jadassohn Lewandowsky Syndrome
- Pachyonychia Congenita Tarda, Type 1
- Type 1 Pachyonychia Congenita
- Pachyonychia Congenita Type 1
- Jadassohn-Lewandowski Syndrome (Pc-1)
- Jadassohn Lewandowski Syndrome (Pc 1)
- Syndrome, Jadassohn-Lewandowski (Pc-1)
- Pachyonychia Congenita, Type 2
- Pachyonychia Congenita, Jackson-Lawler Type
- Pachyonychia Congenita, Jackson Lawler Type
- Jackson-Lawler Type Pachyonychia Congenita
- Jackson Lawler Type Pachyonychia Congenita
- Type 2 Pachyonychia Congenita
- Pachyonychia Congenita Jackson Lawler Type
- Jackson-Lawler Syndrome (Pc-2)
- Jackson Lawler Syndrome (Pc 2)
- Syndrome, Jackson-Lawler (Pc-2)
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