OBSOLETE: Retinitis pigmentosa and intellectual disability due to monosomy Xp11.3
ORPHA:261512Mirhosseini-Holmes-Walton syndrome
ORPHA:3084Mowat-Wilson syndrome due to monosomy 2q22
ORPHA:261537OBSOLETE: Atrichia-intellectual disability and growth delay syndrome
ORPHA:1211OBSOLETE: Grix-Blankenship-Peterson syndrome
ORPHA:2099OBSOLETE: Intellectual disability-hypotonia-skin hyperpigmentation syndrome
ORPHA:3050OBSOLETE: Juvenile parkinsonism with intellectual disability due to DNAJC6 deficiency
ORPHA:352497OBSOLETE: MECP2 duplication syndrome
ORPHA:85281OBSOLETE: Syndromic rod-cone dystrophy
ORPHA:98661OBSOLETE: Trichodermal syndrome-intellectual disability syndrome
ORPHA:3360OBSOLETE: X-linked intellectual disability, Martinez type
ORPHA:775OBSOLETE: X-linked intellectual disability, Raynaud type
ORPHA:3061OBSOLETE: X-linked intellectual disability, Schutz type
ORPHA:3062OBSOLETE: X-linked intellectual disability, Wittner type
ORPHA:3064Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome
ORPHA:3085Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome
ORPHA:436245Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome
ORPHA:3011X-linked intellectual disability-retinitis pigmentosa syndrome
ORPHA:85332