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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
1
I: Photoreceptor Diseases
1
IA: Isolated
1
IA1: Acquired/Progressive
1
IA1a: Retinitis Pigmentosa
1
IA1ai: X-linked
IA1aii: Autosomal Dominant
IA1aiii: Autosomal Recessive
1
SR697
| AR Retinitis Pigmentosa | Gene: USH2A
SR641
| AR Retinitis Pigmentosa | Gene: MAK
SR144
| AR Retinitis Pigmentosa | Gene: USH2A
SR1665
| AR Retinitis Pigmentosa | Gene: USH2A
SR49
| AR Retinitis Pigmentosa | Gene: USH2A
SR816
| AR Retinitis Pigmentosa | Gene: USH2A
SR90
| AR Retinitis Pigmentosa | Gene: USH2A
SR1833
| AR Retinitis Pigmentosa | Gene: FAM161A
SR467
| AR Retinitis Pigmentosa | Gene: FAM161A
SR739
| AR Retinitis Pigmentosa | Gene: FAM161A
SR751
| AR Retinitis Pigmentosa | Gene: FAM161A
SR1832
| AR Retinitis Pigmentosa | Gene: CRB1
SR449
| AR Retinitis Pigmentosa | Gene: CRB1
SR677
| AR Retinitis Pigmentosa | Gene: MAK
SR846
| AR Retinitis Pigmentosa | Gene: MAK
SR1061
| AR Retinitis Pigmentosa | Gene: EYS
SR1745
| AR Retinitis Pigmentosa | Gene: EYS
SR2712
| AR Retinitis Pigmentosa | Gene: EYS
SR172
| AR Retinitis Pigmentosa | Gene: IMPG2
SR18
| AR Retinitis Pigmentosa | Gene: PDE6B
SR364
| AR Retinitis Pigmentosa | Gene: PDE6B
SR71
| AR Retinitis Pigmentosa | Gene: PDE6B
SR568
| AR Retinitis Pigmentosa | Gene: CDHR1
SR1060
| AR Retinitis Pigmentosa | Gene: CERKL
SR1584
| AR Retinitis Pigmentosa | Gene: CERKL
SR318
| AR Retinitis Pigmentosa | Gene: CERKL
SR121
| AR Retinitis Pigmentosa | Gene: CNGB1
SR166
| AR Retinitis Pigmentosa | Gene: DHDDS
SR323
| AR Retinitis Pigmentosa | Gene: MERTK
SR994
| AR Retinitis Pigmentosa | Gene: ZNF408
SR124
| AR Retinitis Pigmentosa | Gene: ABHD12
SR130
| AR Retinitis Pigmentosa | Gene: IFT172
SR118
| AR Retinitis Pigmentosa | Gene: MFRP
SR123
| AR Retinitis Pigmentosa | Gene: SLC24A1
SR136
| AR Retinitis Pigmentosa | Gene: SNRNP200
SR538
| AR Retinitis Pigmentosa | Gene: TULP1
SR1856
| AR Retinitis Pigmentosa | Gene: CNGA1
SR1846
| AR Retinitis Pigmentosa | Gene: REEP6
IA1b: Cone and Cone Rod Dystrophy
IA2: Congenital/Stationary
IB: Syndromic
IB1: Usher Syndrome
IB1a: Type I
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