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| Structural eye disease v0.91 | CSPP1 | Nicola Ragge reviewed gene: CSPP1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.89 | CSPP1 |
Ivone Leong Source NHS GMS was added to CSPP1. Source Expert Review Red was added to CSPP1. Rating Changed from Amber List (moderate evidence) to Red List (low evidence) |
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| Structural eye disease v0.88 | CSPP1 |
Ivone Leong Source Expert Review Amber was added to CSPP1. Rating Changed from Red List (low evidence) to Amber List (moderate evidence) |
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| Structural eye disease v0.60 | CSPP1 | Mariya Moosajee reviewed gene: CSPP1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Joubert syndrome 21; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.59 | CSPP1 |
Ivone Leong gene: CSPP1 was added gene: CSPP1 was added to Structural eye disease. Sources: London North GLH Mode of inheritance for gene: CSPP1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: CSPP1 were set to Joubert syndrome 21, 615636 |
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