Human genes for Tatton-Brown-Rahman syndrome
Tatton-Brown-Rahman syndrome [DOID:0112339]
A syndromic intellectual disability characterized by tall stature, a distinctive facial appearance, and impaired intellectual development that has_material_basis_in heterozygous mutation in DNMT3A on chromosome 2p23.3.
Synonyms: Tatton-Brown-Rahman syndrome, DOID:0112339, TattonBrownRahman syndrome, Tatton-Brown-Rahman disease, Tatton-Brown-Rahman disorder ...