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| Childhood onset dystonia, chorea or related movement disorder v3.56 | KMT2B | Arina Puzriakova Phenotypes for gene: KMT2B were changed from Dystonia 28, childhood-onset 617284; early-onset dystonia to Dystonia 28, childhood-onset, OMIM:617284; Complex early-onset dystonia | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Childhood onset dystonia, chorea or related movement disorder v0.7 | KMT2B |
Ellen McDonagh Source PanelApp was added to KMT2B. Mode of inheritance for gene KMT2B was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Added phenotypes Dystonia 28, childhood-onset 617284; early-onset dystonia for gene: KMT2B Publications for gene KMT2B were changed from to 27992417 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | KMT2B |
Ellen McDonagh gene: KMT2B was added gene: KMT2B was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: KMT2B was set to |
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