Disease Information for Faciogenital Dysplasia Syndrome/FGS1 (Xq12-q21.31)

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Clinical Manifestations
Signs & Symptoms
Cheeks Sunken/Wasting
Facial hemihypertrophy
Associated Diseases & Rule outs
Associated Disease & Complications
Hemihypertrophy
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
Pathophysiology
Pathophysiology/Gene locus Chromosome X.
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Gene locus Xp11.21
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Maternal Chromosome mutation
Process
PROCESS/Eponymic/Esoteric/Not yet integrated into database
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/INCIDENCE/Esoteric disease (example)
Definition

under construction gene locus Xq12-q21.31

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External Links Related to Faciogenital Dysplasia Syndrome/FGS1 (Xq12-q21.31)
Google
Wikipedia
Merck
Images
PubMed (National Library of Medicine)
NGC (National Guideline Clearinghouse)
Medscape (eMedicine)
Harrison's Online (accessmedicine)
NEJM (The New England Journal of Medicine)
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