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 41 ID (Ontology) DOID:0112058 (Human Disease)
Definition A non-syndromic X-linked intellectual disability characterized by mild to moderate intellectual disability that has_material_basis_in heterozygous mutation in the GDI1 gene on chromosome Xq28.
Also Known As "MRX41" ; "MRX48" ; "X-linked mental retardation 41" (for all, see Synonyms field below)
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 Genes
 non-syndromic X-linked intellectual disability 41       1
 for disease ribbon | non-syndromic X-linked intellectual disability 41       1
 model of | non-syndromic X-linked intellectual disability 41       1
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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 41  1 rec.
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Is a non-syndromic X-linked intellectual disability
X-linked dominant disease
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Synonyms
  • "MRX41" EXACT OMO:0003012
    "MRX48" EXACT OMO:0003012
    "X-linked mental retardation 41" EXACT
    "X-linked mental retardation 48" EXACT
Secondary IDs
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MIM:300849