FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term non-syndromic X-linked intellectual disability 19 ID (Ontology) DOID:0112019 (Human Disease)
Definition A non-syndromic X-linked intellectual disability characterized by mild to moderate intellectual disability that has_material_basis_in hemizygous or heterozygous mutation in the RPS6KA3 gene on chromosome Xp22.12.
Also Known As "MRX19" ; "X-linked mental retardation 19"
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 non-syndromic X-linked intellectual disability 19       1
 for disease ribbon | non-syndromic X-linked intellectual disability 19       1
 model of | non-syndromic X-linked intellectual disability 19       1
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__non-syndromic X-linked intellectual disability__
 |__X-linked dominant disease_______________________|
non-syndromic intellectual disability               |
 |__non-syndromic X-linked intellectual disability__|
                                                    non-syndromic X-linked intellectual disability 19  1 rec.
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Is a non-syndromic X-linked intellectual disability
X-linked dominant disease
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Synonyms
  • "MRX19" EXACT OMO:0003012
    "X-linked mental retardation 19" EXACT
Secondary IDs
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MIM:300844