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
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications
- DI
- diagnosis
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology
- GE
- genetics 1
- 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
- UR
- urine
- VE
- veterinary
- VI
- virology
...
Occurrences in Medvik records
C
Diseases
C16.131.077.350.568
Focal Facial Dermal Dysplasias
C16.131.831.350.568
Focal Facial Dermal Dysplasias
C16.320.850.250.568
Focal Facial Dermal Dysplasias
C17.800.804.350.568
Focal Facial Dermal Dysplasias
C17.800.827.250.568
Focal Facial Dermal Dysplasias