Search Ontology:
Human Disease
syndromic X-linked mental retardation 35
- Term ID
- DOID:0080241
- Synonyms
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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/
- References
- Ontology
- Human Disease ( DOID:0080241 )
- is a type of
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