X-Linked Intellectual Disability [mentální retardace vázaná na chromozom X]
topical
17
- Terms
-
mentální retardace vázaná na chromozóm X
syndromy mentální retardace vázané na chromozom X
-
Mental Retardation, X-Linked
X-Linked Mental Retardation
X-Linked Mental Retardation Disorders
X-Linked Mental Retardation Syndromes
Persistent link
https://www.medvik.cz/link/D038901
Definition
A class of genetic disorders resulting in INTELLECTUAL DISABILITY that is associated either with mutations of GENES located on the X CHROMOSOME or aberrations in the structure of the X chromosome (SEX CHROMOSOME ABERRATIONS).
- DUI
- D038901 MeSH Browser
- CUI
- M0417776
- Previous indexing
- Mental Retardation/genetics (1971-2002)
- History note
- 2003
- Public note
- 2003
Allowable subheadings
- BL
- blood 0
- CF
- cerebrospinal fluid 0
- CI
- chemically induced 0
- CL
- classification 1
- CO
- complications 0
- DI
- diagnosis 2
- DG
- diagnostic imaging 0
- DH
- diet therapy 0
- DT
- drug therapy 3
- EC
- economics 0
- EM
- embryology 0
- EN
- enzymology 0
- EP
- epidemiology 0
- EH
- ethnology 0
- ET
- etiology 0
- GE
- genetics 7
- HI
- history 0
- IM
- immunology 1
- ME
- metabolism 1
- MI
- microbiology 0
- MO
- mortality 0
- NU
- nursing 0
- PS
- parasitology 0
- PA
- pathology 1
- PP
- physiopathology 3
- PC
- prevention & control 0
- PX
- psychology 0
- RT
- radiotherapy 0
- RH
- rehabilitation 0
- SU
- surgery 0
- TH
- therapy 1
- UR
- urine 0
- VE
- veterinary 0
- VI
- virology 0
...
Occurrences in Medvik records
C
Diseases
C10.597.606.360.455.249
Coffin-Lowry Syndrome
C16.320.322.030
Aicardi Syndrome
C16.320.322.217
Glycogen Storage Disease Type VIII
C16.320.322.500.249
Coffin-Lowry Syndrome
C16.320.400.525.249
Coffin-Lowry Syndrome