X-linked intellectual disability-retinitis pigmentosa syndrome
ORPHA:85332Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion
ORPHA:261190DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
ORPHA:268261Intellectual disability syndrome due to a DYRK1A point mutation
ORPHA:464311Mirhosseini-Holmes-Walton syndrome
ORPHA:3084Mowat-Wilson syndrome due to a ZEB2 point mutation
ORPHA:261552Mowat-Wilson syndrome due to monosomy 2q22
ORPHA:261537OBSOLETE: Retinitis pigmentosa and intellectual disability due to monosomy Xp11.3
ORPHA:261512Renpenning syndrome
ORPHA:3242Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome
ORPHA:3085Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome
ORPHA:436245SIN3-related intellectual disability syndrome due to a point mutation
ORPHA:500166Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome
ORPHA:3011X-linked intellectual disability due to GRIA3 mutations
ORPHA:364028