Retinitis pigmentosa
ORPHA:791Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome
ORPHA:494439Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome
ORPHA:3085Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome
ORPHA:436245RHYNS syndrome
ORPHA:140976Usher syndrome
ORPHA:886X-linked intellectual disability-retinitis pigmentosa syndrome
ORPHA:85332Autosomal recessive leukoencephalopathy-ischemic stroke-retinitis pigmentosa syndrome
ORPHA:314572Brachydactyly-short stature-retinitis pigmentosa syndrome
ORPHA:166035Cutis verticis gyrata-retinitis pigmentosa-sensorineural deafness syndrome
ORPHA:217315Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome
ORPHA:2235Microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome
ORPHA:251279Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome
ORPHA:2579OBSOLETE: Osteochondrodysplatic nanism-deafness-retinitis pigmentosa syndrome
ORPHA:2653OBSOLETE: Retinitis pigmentosa and intellectual disability due to monosomy Xp11.3
ORPHA:261512Polyneuropathy-hearing loss-ataxia-retinitis pigmentosa-cataract syndrome
ORPHA:171848Posterior column ataxia-retinitis pigmentosa syndrome
ORPHA:88628Primary ciliary dyskinesia-retinitis pigmentosa syndrome
ORPHA:247522Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa
ORPHA:436274Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene
ORPHA:156168Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome
ORPHA:3011Dermatopathia pigmentosa reticularis
ORPHA:86920Lichen planus pigmentosus
ORPHA:254463Maculopapular cutaneous mastocytosis
ORPHA:79457NARP syndrome
ORPHA:644OBSOLETE: Syndromic rod-cone dystrophy
ORPHA:98661