Ichthyosis Vulgaris [ichthyosis vulgaris]

topical
5
Terms

ichthyosis simplex
jednoduchá ichtyóza

 

Ichthyosis Simplex
Ichthyosis Vulgaris, Dominant

Persistent link   https://www.medvik.cz/link/D016112
Definition

Most common form of ICHTHYOSIS characterized by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autosomal dominant trait.

Annotation
do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
DUI
D016112 MeSH Browser
CUI
M0024611
Previous indexing
Ichthyosis (1966-1990)
History note
91
Public note
91

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 1
GE
genetics 1
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy
UR
urine
VE
veterinary
VI
virology

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 749
C16.131.831 Skin Abnormalities 51
C16.131.831.512 Ichthyosis 62
C16.131.831.512.400 Ichthyosiform Erythroderma, Congenital 8
C16.131.831.512.408 Ichthyosis Bullosa of Siemens 3
C16.131.831.512.410 Ichthyosis Vulgaris 5
C16.131.831.512.420 Ichthyosis, X-Linked 9
C16.131.831.512.723 Sjogren-Larsson Syndrome 4
C16.320 Genetic Diseases, Inborn 1 214
C16.320.850 Skin Diseases, Genetic 89
C16.320.850.080 Albinism 17
C16.320.850.180 Cutis Laxa 10
C16.320.850.190 Darier Disease 26
C16.320.850.210 Dermatitis, Atopic 1 452
C16.320.850.235 Dyskeratosis Congenita 9
C16.320.850.250 Ectodermal Dysplasia 33
C16.320.850.260 Ehlers-Danlos Syndrome 51
C16.320.850.275 Epidermolysis Bullosa 108
C16.320.850.337 Erythrokeratodermia Variabilis 1
C16.320.850.368 Hyaline Fibromatosis Syndrome 1
C16.320.850.400 Ichthyosiform Erythroderma, Congenital 8
C16.320.850.402 Ichthyosis Bullosa of Siemens 3
C16.320.850.405 Ichthyosis Vulgaris 5
C16.320.850.408 Ichthyosis, X-Linked 9
C16.320.850.420 Incontinentia Pigmenti 19
C16.320.850.475 Keratoderma, Palmoplantar 15
C16.320.850.542 Leukokeratosis, Hereditary Mucosal 1
C16.320.850.595 Lipoid Proteinosis of Urbach and Wiethe 5
C16.320.850.647 Monilethrix 1
C16.320.850.673 Netherton Syndrome 2
C16.320.850.700 Pemphigus, Benign Familial 11
C16.320.850.730 Porokeratosis 11
C16.320.850.738 Porphyria, Erythropoietic 11
C16.320.850.742 Porphyrias, Hepatic 27
C16.320.850.746 Prolidase Deficiency
C16.320.850.750 Pseudoxanthoma Elasticum 13
C16.320.850.765 Rothmund-Thomson Syndrome 8
C16.320.850.820 Sjogren-Larsson Syndrome 4
C16.320.850.895 Trichothiodystrophy Syndromes 1
C16.320.850.970 Xeroderma Pigmentosum 25
C17 Skin and Connective Tissue Diseases 32
C17.800 Skin Diseases 2 800
C17.800.428 Keratosis 133
C17.800.428.333 Ichthyosis 62
C17.800.428.333.250 Ichthyosiform Erythroderma, Congenital 8
C17.800.428.333.330 Ichthyosis Bullosa of Siemens 3
C17.800.428.333.410 Ichthyosis Vulgaris 5
C17.800.428.333.420 Ichthyosis, X-Linked 9
C17.800.428.333.723 Sjogren-Larsson Syndrome 4
C17.800.804 Skin Abnormalities 51
C17.800.804.512 Ichthyosis 62
C17.800.804.512.400 Ichthyosiform Erythroderma, Congenital 8
C17.800.804.512.405 Ichthyosis Bullosa of Siemens 3
C17.800.804.512.410 Ichthyosis Vulgaris 5
C17.800.804.512.420 Ichthyosis, X-Linked 9
C17.800.804.512.723 Sjogren-Larsson Syndrome 4
C17.800.827 Skin Diseases, Genetic 89
C17.800.827.080 Albinism 17
C17.800.827.180 Cutis Laxa 10
C17.800.827.190 Darier Disease 26
C17.800.827.210 Dermatitis, Atopic 1 452
C17.800.827.235 Dyskeratosis Congenita 9
C17.800.827.250 Ectodermal Dysplasia 33
C17.800.827.260 Ehlers-Danlos Syndrome 51
C17.800.827.275 Epidermolysis Bullosa 108
C17.800.827.337 Erythrokeratodermia Variabilis 1
C17.800.827.368 Hereditary Autoinflammatory Diseases 46
C17.800.827.384 Hyaline Fibromatosis Syndrome 1
C17.800.827.400 Ichthyosiform Erythroderma, Congenital 8
C17.800.827.403 Ichthyosis Bullosa of Siemens 3
C17.800.827.405 Ichthyosis Vulgaris 5
C17.800.827.408 Ichthyosis, X-Linked 9
C17.800.827.420 Incontinentia Pigmenti 19
C17.800.827.475 Keratoderma, Palmoplantar 15
C17.800.827.595 Leukokeratosis, Hereditary Mucosal 1
C17.800.827.602 Monilethrix 1
C17.800.827.610 Muir-Torre Syndrome 10
C17.800.827.655 Netherton Syndrome 2
C17.800.827.700 Pemphigus, Benign Familial 11
C17.800.827.730 Porokeratosis 11
C17.800.827.738 Porphyria, Erythropoietic 11
C17.800.827.742 Porphyrias, Hepatic 27
C17.800.827.750 Pseudoxanthoma Elasticum 13
C17.800.827.775 Rothmund-Thomson Syndrome 8
C17.800.827.820 Sjogren-Larsson Syndrome 4
C17.800.827.895 Trichothiodystrophy Syndromes 1
C17.800.827.970 Xeroderma Pigmentosum 25

Osteosclerosis with ichthyosis and premature ovarian failure Disease MeSH Browser

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