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Disease Atlas
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All Diseases
1
I: Photoreceptor Diseases
1
IA: Isolated
IB: Syndromic
1
IB1: Usher Syndrome
IB2: Bardet Biedl Syndrome
IB3: Neuronal Ceroid Lipofucinosis
IB4: Senior-Loken Syndrome
IB5: Joubert Syndrome
IB6: Microcephaly with or without Chorioretinopathy, Lymphedema
IB7: Retinitis Pigmentosa with Ataxia
IB7a: Posterior Column Ataxia with Retinitis Pigmentosa
SR160
| Posterior Column Ataxia with Retinitis Pigmentosa | Gene: FLVCR1
SR274
| Posterior Column Ataxia with Retinitis Pigmentosa | Gene: FLVCR1
SR83
| Posterior Column Ataxia with Retinitis Pigmentosa | Gene: FLVCR1
IB7b: Spinocerebellar Ataxia 34
IB7c: Neuropathy, Ataxia and Retinitis Pigmentosa
Other Retinitis Pigmentosa with Ataxia
IB8: Peroxisomal Biogenesis Disorders
IB9: Cohen Syndrome
IB10: Retinitis Pigmentosa with Anemia
IB11: Retinitis Pigmentosa with Cognitive Impairment
1
SR3012
| Retinitis Pigmentosa with Cognitive Impairment | Gene: HK1
Other Syndromic
II: Macular Diseases
III: Third Branch Disorders