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| Structural eye disease v0.76 | WDPCP | Nicola Ragge reviewed gene: WDPCP: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ?Bardet-Biedl syndrome 15, 615992; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | WDPCP | Ivone Leong edited their review of gene: WDPCP: Changed phenotypes: ?Bardet-Biedl syndrome 15, 615992 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | WDPCP | Ivone Leong reviewed gene: WDPCP: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Glaucoma 1, open angle, G, 609887; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | WDPCP |
Ivone Leong Source NHS GMS was added to WDPCP. Mode of inheritance for gene WDPCP was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes ?Bardet-Biedl syndrome 15, 615992 for gene: WDPCP |
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| Structural eye disease v0.2 | WDPCP |
Ellen McDonagh gene: WDPCP was added gene: WDPCP was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: WDPCP was set to Phenotypes for gene: WDPCP were set to Eye Disorders |
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