|OBO ID: DOID:0111844|
|Term Name:||X-linked intellectual developmental disorder 108||Search Ontology:|
|Definition:||A non-syndromic X-linked intellectual disability characterized by global developmental delay, delayed walking, and poor speech acquisition that has_material_basis_in hemizygous mutation in SLC9A7 on chromosome Xp11.3. https://www.ncbi.nlm.nih.gov/pubmed/30335141|
|Ontology:||Human Disease (DOID:0111844)|
|is a type of:||
OTHER X-linked intellectual developmental disorder 108 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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