The Maat-Kievit-Brunner type of Ohdo syndrome is a rare condition characterized by intellectual disability and distinctive facial features. It has only been reported in males. The disease is blepharophimosis - intellectual disability syndrome, MKB type (Monarch Disease Ontology id MONDO_0010477). Also known as: BMRS, MKB type, BMRS, Maat-Kievit-Brunner type, Ohdo syndrome, X-linked, X-linked recessive, X-linked Ohdo syndrome, blepharophimosis-intellectual disability syndrome, Maat-Kievit-Brunner type.