Ohdo syndrome and variants congenital nervous system disorder blepharophimosis - intellectual disability syndrome, MKB type https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/ohdo_syndrome_x_linked X-linked Ohdo syndrome MEDGEN:785805 Ohdo syndrome, X-linked, X-linked recessive SCTID:699297004 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. BMRS, MKB type Orphanet:293707 OHDOX MONDO:0010477 GARD:0017341 blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type ICD9:759.89 Ohdo syndrome, X-linked UMLS:C3698541 blepharophimosis-intellectual disability syndrome, Maat-Kievit-Brunner type OMIM:300895 BMRS, Maat-Kievit-Brunner type MED12-related intellectual disability syndrome