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Descriptor English: Pachyonychia Congenita
Descriptor Spanish: Paquioniquia Congénita
Descriptor paquioniquia congénita
Entry term(s) paquioniquia congénita tipo 1
paquioniquia congénita tipo 2
paquioniquia congénita tipo Jackson Lawler
paquioniquia congénita tipo Jackson-Lawler
paquioniquias congénitas
síndrome de Jadassohn Levandowsky
síndrome de Jadassohn Levandowsky (Pc-1)
síndrome de Jadassohn-Levandowsky
Scope note: Grupo de displasias ectodérmicas hereditarias cuya característica clínica más prominente es la distrofia hipertrófica de las uñas, que da lugar a PAQUIONIQUIA. Varios subtipos de paquioniquia congénita se han asociado a mutaciones de genes que codifican QUERATINAS.
Descriptor Portuguese: Paquioníquia Congênita
Descriptor French: Pachyonychie congénitale
Entry term(s): Congenital Pachyonychia
Jackson Lawler Syndrome (Pc 2)
Jackson Lawler Type Pachyonychia Congenita
Jackson-Lawler Syndrome (Pc-2)
Jackson-Lawler Type Pachyonychia Congenita
Jadassohn Lewandowski Syndrome (Pc 1)
Jadassohn Lewandowsky Syndrome
Jadassohn-Lewandowski Syndrome (Pc-1)
Jadassohn-Lewandowsky Syndrome
Pachyonychia Congenita Jackson Lawler Type
Pachyonychia Congenita Syndrome
Pachyonychia Congenita Tarda, Type 1
Pachyonychia Congenita Type 1
Pachyonychia Congenita, Jackson Lawler Type
Pachyonychia Congenita, Jackson-Lawler Type
Pachyonychia Congenita, Jadassohn Lewandowsky Type
Pachyonychia Congenita, Jadassohn-Lewandowsky Type
Pachyonychia Congenita, Type 1
Pachyonychia Congenita, Type 2
Pachyonychia, Congenital
Syndrome, Jackson-Lawler (Pc-2)
Syndrome, Jadassohn-Lewandowski (Pc-1)
Type 1 Pachyonychia Congenita
Type 2 Pachyonychia Congenita
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
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D053549
Scope note: 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.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Nails, Malformed (1964-2006)
Public MeSH Note: 2007
History Note: 2007
Related: Keratin-17 MeSH
Keratin-6 MeSH
Nails, Malformed MeSH
DeCS ID: 52142
Unique ID: D053549
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2007/01/01
Date of Entry: 2006/07/05
Revision Date: 2018/06/14
Pachyonychia Congenita - Preferred
Concept UI M0494472
Scope note 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.
Preferred term Pachyonychia Congenita
Entry term(s) Congenital Pachyonychia
Pachyonychia Congenita Syndrome
Pachyonychia, Congenital
Pachyonychia Congenita, Type 1 - Narrower
Concept UI M0494506
Scope note A subtype of pachyonychia congenita that is associated with mutations in the gene for KERATIN-16 and the gene for KERATIN-6A.
Preferred term Pachyonychia Congenita, Type 1
Entry term(s) Jadassohn Lewandowski Syndrome (Pc 1)
Jadassohn Lewandowsky Syndrome
Jadassohn-Lewandowski Syndrome (Pc-1)
Jadassohn-Lewandowsky Syndrome
Pachyonychia Congenita Tarda, Type 1
Pachyonychia Congenita Type 1
Pachyonychia Congenita, Jadassohn Lewandowsky Type
Pachyonychia Congenita, Jadassohn-Lewandowsky Type
Syndrome, Jadassohn-Lewandowski (Pc-1)
Type 1 Pachyonychia Congenita
Pachyonychia Congenita, Type 2 - Narrower
Concept UI M0494507
Scope note A subtype of pachyonychia congenita that is associated with mutations in the genes for KERATIN-17 or KERATIN-6B.
Preferred term Pachyonychia Congenita, Type 2
Entry term(s) Jackson Lawler Syndrome (Pc 2)
Jackson Lawler Type Pachyonychia Congenita
Jackson-Lawler Syndrome (Pc-2)
Jackson-Lawler Type Pachyonychia Congenita
Pachyonychia Congenita Jackson Lawler Type
Pachyonychia Congenita, Jackson Lawler Type
Pachyonychia Congenita, Jackson-Lawler Type
Syndrome, Jackson-Lawler (Pc-2)
Type 2 Pachyonychia Congenita



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