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| Chromosome Breakage Disorders v2.3 | SMC6 | chirag patel Marked gene: SMC6 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chromosome Breakage Disorders v2.3 | SMC6 | chirag patel Gene: smc6 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chromosome Breakage Disorders v2.3 | chirag patel Copied gene SMC6 from panel Intellectual disability syndromic and non-syndromic | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chromosome Breakage Disorders v2.3 | SMC6 |
chirag patel gene: SMC6 was added gene: SMC6 was added to Chromosome Breakage Disorders. Sources: Expert Review Amber,Other Mode of inheritance for gene: SMC6 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: SMC6 were set to Neurodevelopmental disorder, MONDO:0700092, SMC6-related |
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