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  2. Hydrops fetalis
  3. HADHA
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Hydrops fetalis

Gene: HADHA

Red List (low evidence)
HADHA (hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha)
EnsemblGeneIds (GRCh38): ENSG00000084754
EnsemblGeneIds (GRCh37): ENSG00000084754
OMIM: 600890, Gene2Phenotype
HADHA is in 17 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Gene listed in a review as a cause of fetal hydrops, single case report identified to support link.
Sources: Expert list
Created: 13 Aug 2020, 8:16 a.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
LCHAD deficiency, MIM# 609016

Publications

Created: 13 Aug 2020, 8:16 a.m.

Panel version: 0.130

History Filter Activity

13 Aug 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: hadha has been classified as Red List (Low Evidence).

13 Aug 2020, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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