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Deafness_Isolated v1.9 ALMS1 Zornitza Stark Tag for review was removed from gene: ALMS1.
Deafness_Isolated v1.9 ALMS1 Zornitza Stark edited their review of gene: ALMS1: Added comment: The hearing loss is a relatively early feature, and the eye findings may not be recognised without sub specialist assessment, especially in infants/young children. Included for completeness, particularly for paediatric patients presenting early in the disease trajectory. Gene is included in GEL Hearing Loss panel for same reason.; Changed publications: 11941369, 17594715, 20301444
Deafness_Isolated v1.9 ALMS1 Bryony Thompson Tag for review tag was added to gene: ALMS1.
Deafness_Isolated v1.2 ALMS1 Bryony Thompson reviewed gene: ALMS1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Isolated deafness; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Deafness_Isolated v0.25 ALMS1 Zornitza Stark Marked gene: ALMS1 as ready
Deafness_Isolated v0.25 ALMS1 Zornitza Stark Gene: alms1 has been classified as Green List (High Evidence).
Deafness_Isolated v0.25 ALMS1 Zornitza Stark Phenotypes for gene: ALMS1 were changed from Alstrom syndrome to Alstrom syndrome, MIM# 203800
Deafness_Isolated v0.24 ALMS1 Zornitza Stark Publications for gene: ALMS1 were set to
Deafness_Isolated v0.0 ALMS1 Zornitza Stark gene: ALMS1 was added
gene: ALMS1 was added to DeafnessIsolated. Sources: Melbourne Genomics Health Alliance Deafness Flagship,Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: ALMS1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ALMS1 were set to Alstrom syndrome