Pachyonychia Congenita [pachyonychia congenita]

topical
3
Terms

Jacksonův-Lawlerův syndrom
kongenitální pachyonychie
pachyonychia congenita - typ 1
pachyonychia congenita - typ 2
pachyonychia congenita typu 1
pachyonychia congenita typu 2
pachyonychia congenita typu Jadassohn-Lewandowski
pachyonychie kongenitální
syndrom Jadassohnův-Lewandowského

 

Congenital Pachyonychia
Jackson-Lawler Syndrome (Pc-2)
Jackson-Lawler Type Pachyonychia Congenita
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, Jadassohn-Lewandowsky Type
Pachyonychia Congenita, Type 1
Pachyonychia Congenita, Type 2
Type 1 Pachyonychia Congenita
Type 2 Pachyonychia Congenita

Persistent link   https://www.medvik.cz/link/D053549
Definition

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.

DUI
D053549 MeSH Browser
CUI
M0494472
Previous indexing
Nails, Malformed (1964-2006)
History note
2007
Public note
2007

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
DI
diagnosis 1
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology
GE
genetics 2
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology 1
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 1
UR
urine
VE
veterinary
VI
virology

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 753
C16.131.077 Abnormalities, Multiple 330
C16.131.077.350 Ectodermal Dysplasia 33
C16.131.077.350.198 Ectodermal Dysplasia 1, Anhidrotic 3
C16.131.077.350.298 Ectodermal Dysplasia 3, Anhidrotic 1
C16.131.077.350.348 Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 2
C16.131.077.350.398 Ellis-Van Creveld Syndrome 11
C16.131.077.350.424 Focal Dermal Hypoplasia 6
C16.131.077.350.568 Focal Facial Dermal Dysplasias
C16.131.077.350.712 Neurocutaneous Syndromes 30
C16.131.077.350.856 Pachyonychia Congenita 3
C16.131.831 Skin Abnormalities 51
C16.131.831.350 Ectodermal Dysplasia 33
C16.131.831.350.198 Ectodermal Dysplasia 1, Anhidrotic 3
C16.131.831.350.298 Ectodermal Dysplasia 3, Anhidrotic 1
C16.131.831.350.348 Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 2
C16.131.831.350.398 Ellis-Van Creveld Syndrome 11
C16.131.831.350.424 Focal Dermal Hypoplasia 6
C16.131.831.350.568 Focal Facial Dermal Dysplasias
C16.131.831.350.712 Neurocutaneous Syndromes 30
C16.131.831.350.856 Pachyonychia Congenita 3
C16.131.831.350.856.500 Steatocystoma Multiplex 2
C16.320 Genetic Diseases, Inborn 1 215
C16.320.850 Skin Diseases, Genetic 89
C16.320.850.250 Ectodermal Dysplasia 33
C16.320.850.250.198 Ectodermal Dysplasia 1, Anhidrotic 3
C16.320.850.250.298 Ectodermal Dysplasia 3, Anhidrotic 1
C16.320.850.250.348 Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 2
C16.320.850.250.398 Ellis-Van Creveld Syndrome 11
C16.320.850.250.424 Focal Dermal Hypoplasia 6
C16.320.850.250.568 Focal Facial Dermal Dysplasias
C16.320.850.250.712 Neurocutaneous Syndromes 30
C16.320.850.250.856 Pachyonychia Congenita 3
C16.320.850.250.856.500 Steatocystoma Multiplex 2
C17 Skin and Connective Tissue Diseases 32
C17.800 Skin Diseases 2 801
C17.800.529 Nail Diseases 178
C17.800.529.400 Nail-Patella Syndrome 8
C17.800.529.406 Nails, Ingrown 56
C17.800.529.478 Onycholysis 10
C17.800.529.550 Onychomycosis 277
C17.800.529.594 Pachyonychia Congenita 3
C17.800.529.594.500 Steatocystoma Multiplex 2
C17.800.529.639 Paronychia 24
C17.800.529.819 Yellow Nail Syndrome
C17.800.804 Skin Abnormalities 51
C17.800.804.350 Ectodermal Dysplasia 33
C17.800.804.350.198 Ectodermal Dysplasia 1, Anhidrotic 3
C17.800.804.350.298 Ectodermal Dysplasia 3, Anhidrotic 1
C17.800.804.350.348 Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 2
C17.800.804.350.398 Ellis-Van Creveld Syndrome 11
C17.800.804.350.424 Focal Dermal Hypoplasia 6
C17.800.804.350.568 Focal Facial Dermal Dysplasias
C17.800.804.350.712 Neurocutaneous Syndromes 30
C17.800.804.350.856 Pachyonychia Congenita 3
C17.800.804.350.856.500 Steatocystoma Multiplex 2
C17.800.827 Skin Diseases, Genetic 89
C17.800.827.250 Ectodermal Dysplasia 33
C17.800.827.250.198 Ectodermal Dysplasia 1, Anhidrotic 3
C17.800.827.250.298 Ectodermal Dysplasia 3, Anhidrotic 1
C17.800.827.250.348 Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 2
C17.800.827.250.398 Ellis-Van Creveld Syndrome 11
C17.800.827.250.424 Focal Dermal Hypoplasia 6
C17.800.827.250.568 Focal Facial Dermal Dysplasias
C17.800.827.250.712 Neurocutaneous Syndromes 30
C17.800.827.250.856 Pachyonychia Congenita 3
C17.800.827.250.856.500 Steatocystoma Multiplex 2

Gorlin Bushkell Jensen syndrome Disease MeSH Browser

Pachyonychia congenita recessive Disease MeSH Browser

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