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Childhood onset dystonia, chorea or related movement disorder v0.7 | C2CD3 |
Ellen McDonagh Source PanelApp was added to C2CD3. Mode of inheritance for gene C2CD3 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes MIM208500); MIM 613091, 263520), Jeune asphyxiating thoracic dystrophy (JATD; short-rib polydactyly syndromes (SRPS; ?Orofaciodigital syndrome XIV, 615948; Orofaciodigital syndromes (OFDS, MIM 311200) for gene: C2CD3 Publications for gene C2CD3 were changed from to 26044959; 27094867; 24997988 |
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Childhood onset dystonia, chorea or related movement disorder v0.0 | C2CD3 |
Ellen McDonagh gene: C2CD3 was added gene: C2CD3 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: C2CD3 was set to |