Activity
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| Dystonia, chorea or related movement disorder, childhood onset v0.7 | TMEM138 |
Ellen McDonagh Source PanelApp was added to TMEM138. Mode of inheritance for gene TMEM138 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Joubert syndrome 16; Joubert syndrome with oculorenal defect for gene: TMEM138 Publications for gene TMEM138 were changed from to 22282472 |
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| Dystonia, chorea or related movement disorder, childhood onset v0.0 | TMEM138 |
Ellen McDonagh gene: TMEM138 was added gene: TMEM138 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: TMEM138 was set to |
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