OBO ID: DOID:0080241 |
Term Name: | syndromic X-linked mental retardation 35 | Search Ontology: | |
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Definition: | A syndromic X-linked intellectual disability that has_material_basis_in mutation in the RPL10 gene on chromosome Xq28. https://pubmed.ncbi.nlm.nih.gov/26290468/ | ||
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Ontology: | Human Disease ( DOID:0080241 ) |
OTHER syndromic X-linked mental retardation 35 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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