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Disease Atlas
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Disease Atlas
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Show Cases Added By Recency:
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All Diseases
4
I: Photoreceptor Diseases
4
IA: Isolated
IB: Syndromic
4
IB1: Usher Syndrome
4
IB1a: Type I
4
SR447
| Type 1 Usher Syndrome | Gene: PCDH15
SR1829
| Type 1 Usher Syndrome | Gene: MYO7A
SR487
| Type 1 Usher Syndrome | Gene: MYO7A
SR548
| Type 1 Usher Syndrome | Gene: MYO7A
SR85
| Type 1 Usher Syndrome | Gene: MYO7A
SR573
| Type 1 Usher Syndrome | Gene: CDH23
SR100
| Type 1 Usher Syndrome | Gene: USH1C
SR94
| Type 1 Usher Syndrome | Gene: USH1C
SR96
| Type 1 Usher Syndrome | Gene: USH1C
SR370
| Type 1 Usher Syndrome | Gene: USH1G
IB1b: Type II
IB1c: Type III
Other 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
IB8: Peroxisomal Biogenesis Disorders
IB9: Cohen Syndrome
SR497
| Cohen Syndrome | Gene: VPS13B
SR531
| Cohen Syndrome | Gene: VPS13B
SR597
| Cohen Syndrome | Gene: VPS13B
IB10: Retinitis Pigmentosa with Anemia
IB11: Retinitis Pigmentosa with Cognitive Impairment
Other Syndromic
II: Macular Diseases
III: Third Branch Disorders