Disease Information for Fragile X syndrome/X-linked retardation: Disease Mechanism & Classification

Ads
Class
CLASS/Jablonski/NIH Archive Anomalies Database
CLASS/Pediatric disorders (ex)
CLASS/Systemic/no comment (category)
Pathophysiology
Pathophysiology/Chromosomes fragile
Pathophysiology/Defective DNA repair mechanisms
Pathophysiology/Gene locus Chromosome X.
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Gene locus Xq27.3
Pathophysiology/Gene locus Xq27-q28
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Myocardial Ischemia Non-Arteriosclerosis
Pathophysiology/Maternal Chromosome mutation
Pathophysiology/Gene locus Xq27.8
Process
PROCESS/Chromosomal disorder (ex)
PROCESS/Chromosome breakage syndrome (ex)
PROCESS/Congenital/developmental (category)
PROCESS/Eponymic (category)
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/Hereditofamilial (category)
PROCESS/INCIDENCE/Rare disease (ex)
PROCESS/Multiple dysmorphic syndrome (ex)
PROCESS/Sex-linked (X-linked) recessive inheritance (ex)
PROCESS/Dystostosis/craniofacial (ex)
Ads