| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Proteinuric renal disease v1.170 | SYNPO | Eleanor Williams Phenotypes for gene: SYNPO were changed from to Focal segmental glomerulosclerosis; FSGS | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Proteinuric renal disease v1.169 | SYNPO | Eleanor Williams Publications for gene: SYNPO were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Proteinuric renal disease v1.16 | SYNPO | Eleanor Williams reviewed gene: SYNPO: Rating: AMBER; Mode of pathogenicity: ; Publications: PMID: 19666657; Phenotypes: FSGS; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Proteinuric renal disease v1.15 | SYNPO |
Eleanor Williams gene: SYNPO was added gene: SYNPO was added to Proteinuric renal disease. Sources: NHS GMS Mode of inheritance for gene: SYNPO was set to |
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