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| Intellectual disability syndromic and non-syndromic v2.157 | PUSL1 | Rylee Peters Marked gene: PUSL1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v2.157 | PUSL1 | Rylee Peters Gene: pusl1 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v2.157 | Rylee Peters Copied gene PUSL1 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v2.157 | PUSL1 |
Rylee Peters gene: PUSL1 was added gene: PUSL1 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert Review Amber,Literature Mode of inheritance for gene: PUSL1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: PUSL1 were set to 42598855 Phenotypes for gene: PUSL1 were set to Mitochondrial disease, MONDO:0044970, PUSL1-related |
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