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| Dystonia, chorea or related movement disorder, childhood onset v7.12 | SLC46A1 | Arina Puzriakova Phenotypes for gene: SLC46A1 were changed from Folate malabsorption, hereditary, 229050 to Folate malabsorption, hereditary, OMIM:229050 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dystonia, chorea or related movement disorder, childhood onset v0.1 | SLC46A1 |
Ellen McDonagh Source South West GLH was added to SLC46A1. Mode of inheritance for gene SLC46A1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Folate malabsorption, hereditary, 229050 for gene: SLC46A1 |
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| Dystonia, chorea or related movement disorder, childhood onset v0.0 | SLC46A1 |
Ellen McDonagh gene: SLC46A1 was added gene: SLC46A1 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: SLC46A1 was set to |
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