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Inherited phaeochromocytoma and paraganglioma v1.9 VHL Ivone Leong Phenotypes for gene: VHL were changed from Pheochromocytoma, OMIM:171300 to Pheochromocytoma, OMIM:171300; von Hippel-Lindau syndrome, OMIM:193300
Inherited phaeochromocytoma and paraganglioma v1.8 VHL Ivone Leong Publications for gene: VHL were set to
Inherited phaeochromocytoma and paraganglioma v1.7 VHL Ivone Leong Phenotypes for gene: VHL were changed from von Hippel-Lindau syndrome, 193300Renal cell carcinoma, somatic, 144700Pheochromocytoma, 171300Hemangioblastoma, cerebellar, somaticErythrocytosis, familial, 2, 263400 to Pheochromocytoma, OMIM:171300
Inherited phaeochromocytoma and paraganglioma v1.6 MDH2 Ivone Leong Added comment: Comment on publications: Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene. J. Natl. Cancer Inst. J Natl Cancer Inst 2015 May 11;107(5). Epub 2015 Mar 11.
Inherited phaeochromocytoma and paraganglioma v1.6 MDH2 Ivone Leong Publications for gene: MDH2 were set to Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene. J. Natl. Cancer Inst. J Natl Cancer Inst 2015 May 11; 107(5). Epub 2015 Mar 11.
Inherited phaeochromocytoma and paraganglioma v1.5 PRKAR1A Ivone Leong reviewed gene: PRKAR1A: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Inherited phaeochromocytoma and paraganglioma v1.5 Ivone Leong Panel types changed to Rare Disease 100K
Inherited phaeochromocytoma and paraganglioma v1.3 Ellen McDonagh Panel name changed from Neuro-endocrine Tumours- PCC and PGL to Inherited phaeochromocytoma and paraganglioma
List of related panels changed from to Neuro-endocrine Tumours- PCC and PGL
Panel types changed to Rare Disease 100K; GMS Rare Disease Virtual