Disease #00262 (FXS (syndrome, fragile-X (FXS)), OMIM:300624)

Official abbreviation FXS
Name syndrome, fragile-X (FXS)
OMIM ID 300624
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 4
Phenotype entries for this disease 2
Associated with 1 gene FMR1
Associated tissues -
Disease features -
Remarks X-linked dominant


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00003130 - - - M no Germany;Poland Caucasian - 0 - - FXS - FMR1 FMR1 1 1 Leila Myrick
00295611 - - - M no France - 04y03m 0 - melatonine FXS Intellectual disability, poor attention span, hyperactivities, stereotypies, anxiety and multiple dysmorphic features FMR1 FMR1 1 1 Thierry Bienvenu
00299866 - - - M - - - - 0 - - FXS - - FMR1 1 1 Irma Järvelä
00299867 - - - - - - - - 0 - - FXS - - FMR1 1 1 Irma Järvelä
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