X-linked intellectual disability-retinitis pigmentosa syndrome
ORPHA:85332Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome
ORPHA:352530Mirhosseini-Holmes-Walton syndrome
ORPHA:3084Mowat-Wilson syndrome due to monosomy 2q22
ORPHA:261537OBSOLETE: Retinitis pigmentosa and intellectual disability due to monosomy Xp11.3
ORPHA:261512Rare intellectual disability
ORPHA:87277Renpenning syndrome
ORPHA:3242Retinitis 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 due to GRIA3 mutations
ORPHA:364028X-linked intellectual disability, Abidi type
ORPHA:85273X-linked intellectual disability, Nascimento type
ORPHA:163956X-linked intellectual disability, Pai type
ORPHA:85322X-linked intellectual disability, Raymond type
ORPHA:163953