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Intellectual disability - microarray and sequencing v3.1626 HECW2 Arina Puzriakova Publications for gene: HECW2 were set to 25529582
Intellectual disability - microarray and sequencing v3.868 HECW2 Ivone Leong commented on gene: HECW2
Intellectual disability - microarray and sequencing v3.868 HECW2 Ivone Leong Phenotypes for gene: HECW2 were changed from Neurodevelopmental disorder with hypotonia, seizures, and absent language to Neurodevelopmental disorder with hypotonia, seizures, and absent language, OMIM:617268
Intellectual disability - microarray and sequencing v3.867 HECW2 Ivone Leong Mode of pathogenicity for gene: HECW2 was changed from to Other
Intellectual disability - microarray and sequencing v3.866 HECW2 Ivone Leong Publications for gene: HECW2 were set to
Intellectual disability - microarray and sequencing v3.865 HECW2 Ivone Leong gene: HECW2 was added
gene: HECW2 was added to Intellectual disability. Sources: Expert Review Green,BRIDGE study SPEED NEURO Tier1 Gene,Victorian Clinical Genetics Services
Mode of inheritance for gene: HECW2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: HECW2 were set to Neurodevelopmental disorder with hypotonia, seizures, and absent language
Intellectual disability - microarray and sequencing v3.861 Ivone Leong removed gene:HECW2 from the panel
Intellectual disability - microarray and sequencing v2.468 HECW2 Louise Daugherty Source Victorian Clinical Genetics Services was added to HECW2.
Intellectual disability - microarray and sequencing HECW2 BRIDGE consortium edited their review of HECW2
Intellectual disability - microarray and sequencing HECW2 Louise Daugherty classified HECW2 as amber
Intellectual disability - microarray and sequencing HECW2 Louise Daugherty commented on HECW2
Intellectual disability - microarray and sequencing HECW2 BRIDGE consortium reviewed HECW2