Human genes for Wilson-Turner syndrome
Wilson-Turner syndrome [DOID:0060814]
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.
Synonyms: Wilson-Turner syndrome, DOID:0060814, WilsonTurner syndrome, Wilson-Turner disease, Wilson-Turner disorder ...