Ectodermal Dysplasia 3, Anhidrotic [ektodermální dysplazie 3 anhidrotická]

topical
1
Terms

anhidrotická ektodermální dysplazie 3
ektodermální dysplazie hypohidrotická autozomálně dominantní

 

Ectodermal Dysplasia, Hypohidrotic, Autosomal Dominant

Persistent link   https://www.medvik.cz/link/D053359
Definition

An autosomal dominant form of ectodermal dysplasia which is due to mutations in the gene for the EDAR RECEPTOR.

DUI
D053359 MeSH Browser
CUI
M0492747
Previous indexing
Ectodermal Dysplasia (1987-2006)
History note
2007
Public note
2007

C Diseases
C16.131.077.350 Ectodermal Dysplasia 33
C16.131.077.350.398 Ellis-Van Creveld Syndrome 11
C16.131.077.350.424 Focal Dermal Hypoplasia 6
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
C16.131.831.350.398 Ellis-Van Creveld Syndrome 11
C16.131.831.350.424 Focal Dermal Hypoplasia 6
C16.131.831.350.712 Neurocutaneous Syndromes 29
C16.131.831.350.856 Pachyonychia Congenita 3
C16.320.850.250 Ectodermal Dysplasia 33
C16.320.850.250.398 Ellis-Van Creveld Syndrome 11
C16.320.850.250.424 Focal Dermal Hypoplasia 6
C16.320.850.250.712 Neurocutaneous Syndromes 29
C16.320.850.250.856 Pachyonychia Congenita 3
C17.800 Skin Diseases 2 799
C17.800.804 Skin Abnormalities 51
C17.800.804.350 Ectodermal Dysplasia 33
C17.800.804.350.398 Ellis-Van Creveld Syndrome 11
C17.800.804.350.424 Focal Dermal Hypoplasia 6
C17.800.804.350.712 Neurocutaneous Syndromes 29
C17.800.804.350.856 Pachyonychia Congenita 3
C17.800.827.250 Ectodermal Dysplasia 33
C17.800.827.250.398 Ellis-Van Creveld Syndrome 11
C17.800.827.250.424 Focal Dermal Hypoplasia 6
C17.800.827.250.712 Neurocutaneous Syndromes 29
C17.800.827.250.856 Pachyonychia Congenita 3