Corneal Dystrophy, Juvenile Epithelial of Meesmann [Meesmannova rohovková dystrofie juvenilní epiteliální]
topical
1
- Terms
-
Meesmannova rohovková dystrofie juvenilní epitelová
Meesmannova rohovková epiteliální dystrofie
-
Corneal Dystrophy, Meesmann
Corneal Dystrophy, Meesmann Epithelial
Juvenile Hereditary Epithelial Dystrophy
Meesmann Corneal Dystrophy
Meesmann Corneal Epithelial Dystrophy
Meesmann Epithelial Corneal Dystrophy
Persistent link
https://www.medvik.cz/link/D053559
Definition
An autosomal dominant form of hereditary corneal dystrophy due to a defect in cornea-specific KERATIN formation. Mutations in the genes that encode KERATIN-3 and KERATIN-12 have been linked to this disorder.
- DUI
- D053559 MeSH Browser
- CUI
- M0494580
- Previous indexing
- Cornea (1954-1964); Corneal Dystrophies, Hereditary (1965-2006)
- 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
- 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
...
Occurrences in Medvik records
C
Diseases