OBO ID: DOID:0060817 |
Term Name: | syndromic X-linked intellectual disability 34 | Search Ontology: | |
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Definition: | A syndromic X-linked intellectual disability characterized by delayed psychomotor development, intellectual disability, impaired speech, dysmorphic facial features, and mild structural brain abnormalities, including thickening of the corpus callosum that has_material_basis_in mutation in the NONO gene on chromosome Xq13. https://www.ncbi.nlm.nih.gov/pubmed/26571461 | ||
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Ontology: | Human Disease ( DOID:0060817 ) |
OTHER syndromic X-linked intellectual disability 34 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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NONO | Intellectual developmental disorder, X-linked syndromic 34 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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