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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
cone-rod dystrophy 3 A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the ABCA4 gene on chromosome 1p22. (DO)
Cone-Rod Dystrophy and Hearing Loss +
CONE-ROD SYNAPTIC DISORDER SYNDROME, CONGENITAL NONPROGRESSIVE
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities
dominant pericentral pigmentary retinopathy
Furukawa Takagi Nakao Syndrome
INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA
isolated microphthalmia 5
late-adult onset retinitis pigmentosa
Leber congenital amaurosis 14
Leber congenital amaurosis 3
Macular Dystrophy with Central Cone Involvement
Metaphyseal Chondrodysplasia with Retinitis Pigmentosa
Microcephaly, Retinitis Pigmentosa, and Sutural Cataract
Microcornea, Rod-Cone Dystrophy, Cataract, and Posterior Staphyloma 1
Mirhosseini-Holmes-Walton Syndrome
multiple congenital anomalies-hypotonia-seizures syndrome 3
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus
Newfoundland cone-rod dystrophy
Oliver-McFarlane syndrome
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
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
Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction
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
Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation
spondylometaphyseal dysplasia with cone-rod dystrophy
Tapetoretinal Degeneration with Ataxia
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 retinitis pigmentosa and sinorespiratory infections
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