OBO ID: DOID:0111844 |
Term Name: | X-linked intellectual developmental disorder 108 | Search Ontology: | |
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Definition: | A syndromic X-linked intellectual disability characterized by global developmental delay, delayed walking, and poor speech acquisition that has_material_basis_in hemizygous mutation in the SLC9A7 gene on chromosome Xp11.3. https://www.ncbi.nlm.nih.gov/pubmed/30335141 | ||
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Ontology: | Human Disease ( DOID:0111844 ) |
OTHER X-linked intellectual developmental disorder 108 PAGES
ZEBRAFISH MODELS
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PHENOTYPE
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CITATIONS: None
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