Activity

Filter

Cancel
Date Panel Item Activity
5 actions
Dystonia, chorea or related movement disorder, childhood onset v7.11 DLD Arina Puzriakova Phenotypes for gene: DLD were changed from Dihydrolipoamide dehydrogenase deficiency, 246900 to Dihydrolipoamide dehydrogenase deficiency, OMIM:246900
Dystonia, chorea or related movement disorder, childhood onset v0.207 DLD Louise Daugherty Phenotypes for gene: DLD were changed from Dihydrolipoamide dehydrogenase deficiency to Dihydrolipoamide dehydrogenase deficiency, 246900
Dystonia, chorea or related movement disorder, childhood onset v0.45 DLD Ellen McDonagh Phenotypes for gene: DLD were changed from to Dihydrolipoamide dehydrogenase deficiency
Dystonia, chorea or related movement disorder, childhood onset v0.44 DLD Ellen McDonagh Mode of inheritance for gene: DLD was changed from to BIALLELIC, autosomal or pseudoautosomal
Dystonia, chorea or related movement disorder, childhood onset v0.0 DLD Ellen McDonagh gene: DLD was added
gene: DLD was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green
Mode of inheritance for gene: DLD was set to