OBO ID: DOID:0112059 |
Term Name: | non-syndromic X-linked intellectual disability 72 | Search Ontology: | |
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Definition: | A non-syndromic X-linked intellectual disability that has_material_basis_in hemizygous mutation in the RAB39B gene on chromosome Xq28. (2) | ||
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Ontology: | Human Disease ( DOID:0112059 ) |
OTHER non-syndromic X-linked intellectual disability 72 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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