Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Congenital ophthalmoplegia v0.37 | MGME1 | Zornitza Stark Marked gene: MGME1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Congenital ophthalmoplegia v0.37 | MGME1 | Zornitza Stark Gene: mgme1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Congenital ophthalmoplegia v0.37 | MGME1 | Zornitza Stark Classified gene: MGME1 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Congenital ophthalmoplegia v0.37 | MGME1 | Zornitza Stark Gene: mgme1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Congenital ophthalmoplegia v0.36 | MGME1 |
Zornitza Stark gene: MGME1 was added gene: MGME1 was added to Congenital ophthalmoplegia. Sources: Expert list Mode of inheritance for gene: MGME1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: MGME1 were set to Mitochondrial DNA depletion syndrome 11, MIM#615084 Review for gene: MGME1 was set to GREEN Added comment: Onset in the first decade, and progressive external ophthalmoplegia is a prominent feature. Sources: Expert list |