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Date	Panel	Item	Activity
Filter activities 4 actions
09 Dec 2019	Childhood onset dystonia, chorea or related movement disorder v0.228	HCFC1	Louise Daugherty Phenotypes for gene: HCFC1 were changed from Mental retardation, X-linked 3 (methylmalonic acidemia and homocysteinemia, cblX type ) to Mental retardation, X-linked 3 (methylmalonic acidemia and homocysteinemia, cblX type ), 309541
06 Dec 2019	Childhood onset dystonia, chorea or related movement disorder v0.61	HCFC1	Ellen McDonagh Phenotypes for gene: HCFC1 were changed from to Mental retardation, X-linked 3 (methylmalonic acidemia and homocysteinemia, cblX type )
06 Dec 2019	Childhood onset dystonia, chorea or related movement disorder v0.60	HCFC1	Ellen McDonagh Mode of inheritance for gene: HCFC1 was changed from to X-LINKED: hemizygous mutation in males, biallelic mutations in females
06 Dec 2019	Childhood onset dystonia, chorea or related movement disorder v0.0	HCFC1	Ellen McDonagh gene: HCFC1 was added gene: HCFC1 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: HCFC1 was set to