Among these, three were OMIM-annotated:ZMYND11 (associated with autosomal dominant intellectualdevelopmental disorder 30 [AD]), WDR37 (linked toneurooculo-cardiogenitourinary syndrome [AD]), PITRM1(implicated in autosomal recessive spinocerebellar ataxia 30[AR]). The gene discussed is ZMYND11; the disease is spinocerebellar ataxia, autosomal recessive 30.