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Hydrops fetalis v0.131 HADHB Zornitza Stark Marked gene: HADHB as ready
Hydrops fetalis v0.131 HADHB Zornitza Stark Gene: hadhb has been classified as Red List (Low Evidence).
Hydrops fetalis v0.131 HADHB Zornitza Stark gene: HADHB was added
gene: HADHB was added to Hydrops fetalis. Sources: Expert list
Mode of inheritance for gene: HADHB was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: HADHB were set to 26070998
Phenotypes for gene: HADHB were set to Trifunctional protein deficiency, MIM# 609015
Review for gene: HADHB was set to RED
Added comment: Single case reported with prenatal onset cardiomyopathy and hydrops.
Sources: Expert list
Hydrops fetalis v0.130 HADHA Zornitza Stark Marked gene: HADHA as ready
Hydrops fetalis v0.130 HADHA Zornitza Stark Gene: hadha has been classified as Red List (Low Evidence).
Hydrops fetalis v0.130 HADHA Zornitza Stark gene: HADHA was added
gene: HADHA was added to Hydrops fetalis. Sources: Expert list
Mode of inheritance for gene: HADHA was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: HADHA were set to 23137060; 11111210
Phenotypes for gene: HADHA were set to LCHAD deficiency, MIM# 609016
Review for gene: HADHA was set to RED
Added comment: Gene listed in a review as a cause of fetal hydrops, single case report identified to support link.
Sources: Expert list
Hydrops fetalis v0.129 HADH Zornitza Stark Marked gene: HADH as ready
Hydrops fetalis v0.129 HADH Zornitza Stark Gene: hadh has been classified as Red List (Low Evidence).
Hydrops fetalis v0.129 HADH Zornitza Stark gene: HADH was added
gene: HADH was added to Hydrops fetalis. Sources: Expert list
Mode of inheritance for gene: HADH was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: HADH were set to 3-hydroxyacyl-CoA dehydrogenase deficiency, MIM# 231530
Review for gene: HADH was set to RED
Added comment: Cannot find specific reports of hydrops associated with this metabolic disorder.
Sources: Expert list