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Congenital ophthalmoplegia v0.75 SUCLA2 Zornitza Stark Marked gene: SUCLA2 as ready
Congenital ophthalmoplegia v0.75 SUCLA2 Zornitza Stark Gene: sucla2 has been classified as Green List (High Evidence).
Congenital ophthalmoplegia v0.75 SUCLA2 Zornitza Stark Phenotypes for gene: SUCLA2 were changed from to Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) OMIM 612073
Congenital ophthalmoplegia v0.74 SUCLA2 Zornitza Stark Classified gene: SUCLA2 as Green List (high evidence)
Congenital ophthalmoplegia v0.74 SUCLA2 Zornitza Stark Gene: sucla2 has been classified as Green List (High Evidence).
Congenital ophthalmoplegia v0.73 SUCLA2 Shannon LeBlanc reviewed gene: SUCLA2: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 20301762; Phenotypes: Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) OMIM 612073; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital ophthalmoplegia v0.73 SUCLA2 Shannon LeBlanc Deleted their review
Congenital ophthalmoplegia v0.73 SUCLA2 Shannon LeBlanc gene: SUCLA2 was added
gene: SUCLA2 was added to Congenital ophthalmoplegia. Sources: Literature
Mode of inheritance for gene: SUCLA2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SUCLA2 were set to PMID: 20301762
Review for gene: SUCLA2 was set to GREEN
Added comment: Infantile onset. External ophthalmoplegia is feature in up to 25% of patients.
Sources: Literature