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| Childhood onset dystonia, chorea or related movement disorder v1.256 | FASTKD2 | Arina Puzriakova Phenotypes for gene: FASTKD2 were changed from Dystonia to Combined oxidative phosphorylation deficiency 44, OMIM:618855; Dystonia | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Childhood onset dystonia, chorea or related movement disorder v1.255 | FASTKD2 | Arina Puzriakova Phenotypes for gene: FASTKD2 were changed from Dystonia to Dystonia | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Childhood onset dystonia, chorea or related movement disorder v1.254 | FASTKD2 | Arina Puzriakova Mode of inheritance for gene: FASTKD2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Childhood onset dystonia, chorea or related movement disorder v0.1 | FASTKD2 |
Ellen McDonagh Source South West GLH was added to FASTKD2. Mode of inheritance for gene FASTKD2 was changed from to Unknown Added phenotypes Dystonia for gene: FASTKD2 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | FASTKD2 |
Ellen McDonagh gene: FASTKD2 was added gene: FASTKD2 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: FASTKD2 was set to |
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