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| Callosome v1.2 | FSD1L | Zornitza Stark Marked gene: FSD1L as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Callosome v1.2 | FSD1L | Zornitza Stark Gene: fsd1l has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Callosome v1.2 | Zornitza Stark Copied gene FSD1L from panel Intellectual disability syndromic and non-syndromic | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Callosome v1.2 | FSD1L |
Zornitza Stark gene: FSD1L was added gene: FSD1L was added to Callosome. Sources: Expert Review Green,Other Mode of inheritance for gene: FSD1L was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: FSD1L were set to 41720098 Phenotypes for gene: FSD1L were set to Neurodevelopmental disorder with seizures, spastic tetraparesis, and vision impairment, MIM# 621643 |
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