Choroideremia [choroideremie]
topical
3
- Terms
-
choroiderémie
-
Progressive Tapetochoroidal Dystrophy
Tapetochoroidal Dystrophy, Progressive
Persistent link
https://www.medvik.cz/link/D015794
Definition
An X chromosome-linked abnormality characterized by atrophy of the choroid and degeneration of the retinal pigment epithelium causing night blindness.
- Annotation
- of the eye, not of the choroid plexus: progressive degen in male, nonprogressive in female
- DUI
- D015794 MeSH Browser
- CUI
- M0024194
- Previous indexing
- Choroid (1966-1989); Eye Diseases (1966-1974); Uveal Diseases/genetics (1977-1989)
- History note
- 90
- Public note
- 90
Allowable subheadings
- BL
- blood 0
- CF
- cerebrospinal fluid 0
- CI
- chemically induced 0
- CL
- classification 0
- CO
- complications 0
- DI
- diagnosis 0
- DG
- diagnostic imaging 0
- DH
- diet therapy 0
- DT
- drug therapy 0
- EC
- economics 0
- EM
- embryology 0
- EN
- enzymology 0
- EP
- epidemiology 0
- EH
- ethnology 0
- ET
- etiology 1
- GE
- genetics 1
- HI
- history 0
- IM
- immunology 0
- ME
- metabolism 0
- MI
- microbiology 0
- MO
- mortality 0
- NU
- nursing 0
- PS
- parasitology 0
- PA
- pathology 1
- PP
- physiopathology 0
- PC
- prevention & control 0
- PX
- psychology 0
- RT
- radiotherapy 0
- RH
- rehabilitation 0
- SU
- surgery 0
- TH
- therapy 0
- UR
- urine 0
- VE
- veterinary 0
- VI
- virology 0
...
Occurrences in Medvik records
C
Diseases
C11.270.019
Aicardi Syndrome
C11.270.151
Cone Dystrophy
C11.270.152
Cone-Rod Dystrophies
C11.270.238
Familial Exudative Vitreoretinopathies
C11.941.160.241
Choroidal Effusions
C16.320.290.019
Aicardi Syndrome
C16.320.290.152
Cone-Rod Dystrophies
C16.320.290.352
Familial Exudative Vitreoretinopathies
C16.320.322.030
Aicardi Syndrome
C16.320.322.217
Glycogen Storage Disease Type VIII