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Deafness_Isolated v1.13 ELMOD3 Zornitza Stark Phenotypes for gene: ELMOD3 were changed from Deafness, autosomal dominant; Deafness, autosomal recessive 88, MIM# 615429 to Deafness, autosomal dominant 81, MIM# 619500; Deafness, autosomal recessive 88, MIM# 615429
Deafness_Isolated v1.12 ELMOD3 Zornitza Stark edited their review of gene: ELMOD3: Changed phenotypes: Deafness, autosomal recessive 88, MIM# 615429, Deafness, autosomal dominant 81, MIM# 619500
Deafness_Isolated v0.182 ELMOD3 Zornitza Stark Marked gene: ELMOD3 as ready
Deafness_Isolated v0.182 ELMOD3 Zornitza Stark Gene: elmod3 has been classified as Amber List (Moderate Evidence).
Deafness_Isolated v0.0 ELMOD3 Zornitza Stark gene: ELMOD3 was added
gene: ELMOD3 was added to DeafnessIsolated. Sources: Expert Review Amber,Melbourne Genomics Health Alliance Deafness Flagship,Victorian Clinical Genetics Services
Mode of inheritance for gene: ELMOD3 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: ELMOD3 were set to 31628468; 30284680; 24039609; 29713870
Phenotypes for gene: ELMOD3 were set to Deafness, autosomal dominant; Deafness, autosomal recessive 88, MIM# 615429