|OBO ID: DOID:0080984|
|Term Name:||X-linked intellectual developmental disorder 109||Search Ontology:|
|Definition:||A syndromic X-linked intellectual disability characterized by mildly to moderately impaired intellectual development associated with learning difficulties, communication deficits, attention problems, hyperactivity, and autistic behavior and that has_material_basis_in disruption of the FMR2 gene (AFF2, either by expansion of a CCG repeat in the 5-prime untranslated region or by deletion. https://pubmed.ncbi.nlm.nih.gov/21739600/|
|Ontology:||Human Disease (DOID:0080984)|
|is a type of:||
OTHER X-linked intellectual developmental disorder 109 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.