DISEASES

Disease-gene associations mined from literature

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 ...