FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Wilson-Turner syndrome ID (Ontology) DOID:0060814 (Human Disease)
Definition A syndromic X-linked intellectual disability characterized by intellectual disability, truncal obesity, gynecomastia, hypogonadism, dysmorphic facial features, and short stature that has_material_basis_in hemizygous mutation in the LAS1L gene on chromosome Xq12.
Also Known As "mental retardation, X-linked, syndromic 6" ; "mental retardation, X-linked, with gynecomastia and obesity" ; "MRXS6" (for all, see Synonyms field below)
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 Genes
 Wilson-Turner syndrome       1
 for disease ribbon | Wilson-Turner syndrome       1
 model of | Wilson-Turner syndrome       1
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__syndromic X-linked intellectual disability__
 |__X-linked recessive disease__________________|
syndromic intellectual disability               |
 |__syndromic X-linked intellectual disability__|
                                                Wilson-Turner syndrome  1 rec.
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Is a syndromic X-linked intellectual disability
X-linked recessive disease
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Synonyms
  • "mental retardation, X-linked, syndromic 6" EXACT
    "mental retardation, X-linked, with gynecomastia and obesity" EXACT
    "MRXS6" EXACT OMO:0003012
    "WTS" EXACT OMO:0003012
    "X-linked intellectual disability-gynecomastia-obesity syndrome" EXACT
Secondary IDs
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GARD:5579
MIM:309585
ORDO:3459