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| Childhood onset dystonia, chorea or related movement disorder v0.7 | FA2H |
Ellen McDonagh Source PanelApp was added to FA2H. Mode of inheritance for gene FA2H was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes fatty acid hydroxylase-associated neurodegeneration; Dystonia; Spastic paraplegia 35, autosomal recessive 612319 for gene: FA2H Publications for gene FA2H were changed from to 19068277 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | FA2H |
Ellen McDonagh gene: FA2H was added gene: FA2H was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: FA2H was set to |
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