Ectodermal Dysplasia 1, Anhidrotic [ektodermální dysplazie 1 anhidrotická]

topical
3
Terms

Christův-Siemensův-Touraineův syndrom
X-vázaná anhidrotická ektodermální dysplazie
X-vázaná hypohidrotická ektodermální dysplazie

 

Anhidrotic Ectodermal Dysplasia, X-Linked
Anhydrotic Ectodermal Dysplasia, X-Linked
Christ-Siemens-Touraine Syndrome
CST Syndrome
Ectodermal Dysplasia 1
Ectodermal Dysplasia 1, Anhydrotic
Ectodermal Dysplasia, Anhidrotic, X-Linked
Ectodermal Dysplasia, Hypohidrotic, X-Linked
Ectodermal Dysplasia, Hypohydridic, X-Linked
Hypohidrotic Ectodermal Dysplasia
X-Linked Hypohydridic Ectodermal Dysplasia

Persistent link   https://www.medvik.cz/link/D053358
Definition

An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN.

DUI
D053358 MeSH Browser
CUI
M0007033
History note
2007(1993)
Public note
2007; see ECTODERMAL DYSPLASIA 1993-2006

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
DI
diagnosis 2
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology
GE
genetics 3
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 2
UR
urine
VE
veterinary
VI
virology

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 741
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 29
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 29
C16.131.831.350.856 Pachyonychia Congenita 3
C16.320 Genetic Diseases, Inborn 1 213
C16.320.322 Genetic Diseases, X-Linked 59
C16.320.322.030 Aicardi Syndrome
C16.320.322.061 Androgen-Insensitivity Syndrome 56
C16.320.322.068 Barth Syndrome 6
C16.320.322.076 Bulbo-Spinal Atrophy, X-Linked 8
C16.320.322.092 Choroideremia 3
C16.320.322.100 Dent Disease 1
C16.320.322.108 Dyskeratosis Congenita 9
C16.320.322.116 Ectodermal Dysplasia 1, Anhidrotic 3
C16.320.322.124 Fabry Disease 187
C16.320.322.186 Focal Dermal Hypoplasia 6
C16.320.322.201 Glycogen Storage Disease Type IIb 11
C16.320.322.217 Glycogen Storage Disease Type VIII
C16.320.322.233 Granulomatous Disease, Chronic 54
C16.320.322.235 Hemophilia B 214
C16.320.322.237 Hyper-IgM Immunodeficiency Syndrome, Type 1 2
C16.320.322.241 Ichthyosis, X-Linked 9
C16.320.322.370 Isolated Noncompaction of the Ventricular Myocardium 11
C16.320.322.500 X-Linked Intellectual Disability 17
C16.320.322.562 Muscular Dystrophy, Duchenne 133
C16.320.322.625 Muscular Dystrophy, Emery-Dreifuss 18
C16.320.322.750 Oculocerebrorenal Syndrome 9
C16.320.322.828 Ornithine Carbamoyltransferase Deficiency Disease 19
C16.320.322.906 Pelizaeus-Merzbacher Disease 11
C16.320.322.937 Wiskott-Aldrich Syndrome 20
C16.320.322.968 X-Linked Combined Immunodeficiency Diseases 4
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 29
C16.320.850.250.856 Pachyonychia Congenita 3
C17 Skin and Connective Tissue Diseases 32
C17.800 Skin Diseases 2 799
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 29
C17.800.804.350.856 Pachyonychia Congenita 3
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 29
C17.800.827.250.856 Pachyonychia Congenita 3

Hypodontia, X-linked Disease MeSH Browser

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