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Possible mitochondrial disorder, nuclear genes v3.113 HADHB Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HADHB.
Possible mitochondrial disorder, nuclear genes v3.113 HADHB Achchuthan Shanmugasundram commented on gene: HADHB: The rating of this gene has been updated to green following NHS Genomic Medicine Service approval.
Possible mitochondrial disorder, nuclear genes v3.112 HADHB Achchuthan Shanmugasundram Source Expert Review Green was added to HADHB.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Possible mitochondrial disorder, nuclear genes v3.73 HADHB Achchuthan Shanmugasundram Classified gene: HADHB as Amber List (moderate evidence)
Possible mitochondrial disorder, nuclear genes v3.73 HADHB Achchuthan Shanmugasundram Added comment: Comment on list classification: There is sufficient evidence available for the promotion of this gene to green rating in the next GMS review.
Possible mitochondrial disorder, nuclear genes v3.73 HADHB Achchuthan Shanmugasundram Gene: hadhb has been classified as Amber List (Moderate Evidence).
Possible mitochondrial disorder, nuclear genes v3.72 HADHB Achchuthan Shanmugasundram Phenotypes for gene: HADHB were changed from Trifunctional protein deficiency, 609015 to Mitochondrial trifunctional protein deficiency 2, OMIM:620300
Possible mitochondrial disorder, nuclear genes v3.71 HADHB Achchuthan Shanmugasundram Publications for gene: HADHB were set to
Possible mitochondrial disorder, nuclear genes v3.70 HADHB Achchuthan Shanmugasundram Tag Q4_23_promote_green tag was added to gene: HADHB.
Possible mitochondrial disorder, nuclear genes v3.70 HADHB Achchuthan Shanmugasundram reviewed gene: HADHB: Rating: GREEN; Mode of pathogenicity: None; Publications: 35403730; Phenotypes: Mitochondrial trifunctional protein deficiency 2, OMIM:620300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Possible mitochondrial disorder, nuclear genes v0.5 HADHB Ivone Leong reviewed gene: HADHB: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Trifunctional protein deficiency, 609015; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Possible mitochondrial disorder, nuclear genes v0.4 HADHB Ivone Leong gene: HADHB was added
gene: HADHB was added to Possible mitochondrial disorder - nuclear genes. Sources: Expert Review Red,NHS GMS
Mode of inheritance for gene: HADHB was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: HADHB were set to Trifunctional protein deficiency, 609015