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Intellectual disability - microarray and sequencing v3.1538 GDAP1 Arina Puzriakova Mode of inheritance for gene: GDAP1 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Intellectual disability - microarray and sequencing v3.1537 GDAP1 Arina Puzriakova Phenotypes for gene: GDAP1 were changed from Charcot-Marie-Tooth disease, type 4A, 214400; Charcot-Marie-Tooth; disease, axonal, with vocal cord paresis, 607706; Charcot-Marie-Tooth disease, axonal, type 2K, 607831; Charcot-Marie-Tooth disease, recessive; intermediate, A, 608340 to Charcot-Marie-Tooth disease, axonal, type 2K, OMIM:607831; Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, OMIM:607706; Charcot-Marie-Tooth disease, recessive intermediate, A, OMIM:608340; Charcot-Marie-Tooth disease, type 4A, OMIM:214400
Intellectual disability - microarray and sequencing v3.876 GDAP1 Sarah Leigh Source: Expert Review Amber was removed from gene: GDAP1
Intellectual disability - microarray and sequencing GDAP1 BRIDGE consortium edited their review of GDAP1
Intellectual disability - microarray and sequencing GDAP1 BRIDGE consortium edited their review of GDAP1
Intellectual disability - microarray and sequencing GDAP1 Louise Daugherty classified GDAP1 as amber
Intellectual disability - microarray and sequencing GDAP1 Louise Daugherty commented on GDAP1
Intellectual disability - microarray and sequencing GDAP1 BRIDGE consortium reviewed GDAP1