|OBO ID: DOID:0112038|
|Term Name:||non-syndromic X-linked intellectual disability 1||Search Ontology:|
|Definition:||A non-syndromic X-linked intellectual disability characterized by moderate to severe intellectual disability in males and varying levels of intellectual disability in females that has_material_basis_in hemizygous or heterozygous mutation in IQSEC2 on chromosome Xp11.22. (2)|
|Ontology:||Human Disease (DOID:0112038)|
|is a type of:||
OTHER non-syndromic X-linked intellectual disability 1 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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