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| Childhood onset dystonia, chorea or related movement disorder v3.76 | GLI3 | Arina Puzriakova Phenotypes for gene: GLI3 were changed from Joubert Syndrome and Senior-Loken Syndrome 24 gene panel to Greig cephalopolysyndactyly syndrome, OMIM:175700; Pallister-Hall syndrome, OMIM:146510 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Childhood onset dystonia, chorea or related movement disorder v0.7 | GLI3 |
Ellen McDonagh Source PanelApp was added to GLI3. Mode of inheritance for gene GLI3 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Added phenotypes Joubert Syndrome and Senior-Loken Syndrome 24 gene panel for gene: GLI3 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | GLI3 |
Ellen McDonagh gene: GLI3 was added gene: GLI3 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: GLI3 was set to |
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