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| Macular Dystrophy/Stargardt Disease v1.2 | XXYLT1 | Zornitza Stark Marked gene: XXYLT1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Macular Dystrophy/Stargardt Disease v1.2 | XXYLT1 | Zornitza Stark Gene: xxylt1 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Macular Dystrophy/Stargardt Disease v1.2 | Zornitza Stark Copied gene XXYLT1 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Macular Dystrophy/Stargardt Disease v1.2 | XXYLT1 |
Zornitza Stark gene: XXYLT1 was added gene: XXYLT1 was added to Macular Dystrophy/Stargardt Disease. Sources: Expert Review Amber,Literature founder tags were added to gene: XXYLT1. Mode of inheritance for gene: XXYLT1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: XXYLT1 were set to 42530953 Phenotypes for gene: XXYLT1 were set to Inherited retinal dystrophy, MONDO:0019118, XXYLT1-related |
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