| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Early-onset Dementia v2.11 | Bryony Thompson Copied gene SARDH from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Early-onset Dementia v2.11 | SARDH |
Bryony Thompson gene: SARDH was added gene: SARDH was added to Early-onset Dementia. Sources: Expert Review Amber,Expert Review Amber,Literature,Victorian Clinical Genetics Services Mode of inheritance for gene: SARDH was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SARDH were set to 22825317; 27604308 Phenotypes for gene: SARDH were set to Sarcosinemia MIM#268900; Disorders of serine, glycine or glycerate metabolism |
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