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autosomal recessive pericentral pigmentary retinopathy
Bork Stender Schmidt Syndrome
Chang Davidson Carlson Syndrome
Chromosome Xp11.3 Deletion Syndrome
Concentric Annular Macular Dystrophy
Cone Rod Dystrophy Amelogenesis Imperfecta
congenital hypotrichosis with juvenile macular dystrophy
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities
degeneration of macula and posterior pole +
dominant pericentral pigmentary retinopathy
ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome
Furukawa Takagi Nakao Syndrome
INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA
isolated microphthalmia 5
Kuhnt-Junius degeneration +
late-adult onset retinitis pigmentosa
Leber congenital amaurosis 14
Leber congenital amaurosis 3
Macular Degeneration, Early-Onset
Macular Dystrophy with Central Cone Involvement
Macular Dystrophy, Fenestrated Sheen Type
Metaphyseal Chondrodysplasia with Retinitis Pigmentosa
Microcephaly, Retinitis Pigmentosa, and Sutural Cataract
Mirhosseini-Holmes-Walton Syndrome
multiple congenital anomalies-hypotonia-seizures syndrome 3
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders
Newfoundland cone-rod dystrophy
Oliver-McFarlane syndrome
patterned macular dystrophy +
Peripheral Cone Dystrophy
Pigmentary Retinopathy and Sensorineural Deafness
Posterior Column Ataxia with Retinitis Pigmentosa
Progressive Pallidal Degeneration with Retinitis Pigmentosa
Radioulnar Synostosis Retinal Pigment Abnormalities
retinal cone dystrophy 3A
retinal cone dystrophy 3B
retinal macular dystrophy +
RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS
Retinitis Pigmentosa Inversa with Deafness
retinitis pigmentosa with or without situs inversus
Retinitis Pigmentosa with Paraarteriolar Preservation Of Retinal Pigment Epithelium
retinitis pigmentosa Y-linked
Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism
Retinitis Pigmentosa, Late-Onset Dominant
Rhizomelic Dysplasia, Scoliosis, and Retinitis Pigmentosa
Rhizomelic Skeletal Dysplasia with Retinitis Pigmentosa
Severe Mental Retardation, with Spasticity and Pigmentary Tapetoretinal Degeneration
short stature, hearing loss, retinitis pigmentosa, and distinctive facies
short-rib thoracic dysplasia 9 with or without polydactyly
Sorsby's fundus dystrophy
Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation
spondylometaphyseal dysplasia with cone-rod dystrophy
Stargardt Macular Degeneration Absent or Hypoplastic Corpus Callosum Mental Retardation and Dysmorphic Features
Tapetoretinal Degeneration with Ataxia
vitelliform macular dystrophy +
X-Linked Cone Dystrophy with Tapetal-like Sheen
X-linked cone-rod dystrophy 1
X-linked cone-rod dystrophy 2
X-linked cone-rod dystrophy 3
X-Linked Macular Dystrophy +
X-linked retinitis pigmentosa and sinorespiratory infections
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