Fetal hydrops

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 19 panels

1 review

Rebecca Foulger (Genomics England curator)

PMID:23137060 list LCHAD as a non-lysosomal inborn error of metabolism associated with NIHF (Table 3). PMID:11111210 present a case where at 31 weeks of gestation the fetus developed a cardiomegaly and a hydrops; LCHAD deficiency was diagnosed.
Created: 21 Dec 2016, 11:49 a.m.

History Filter Activity

21 Dec 2016, Gel status: 0

panel promoted to version 1

Rebecca Foulger (Genomics England curator)

21 December 2016. External reviews were assessed, and panel was revised according to expert review, internal discussion and additional curation. Following internal discussion, all genes from the V1.14 'RASopathies' panel were added as green EXCLUDING NF1 and SPRED1- a cautious approach was taken because Fetal hydrops is a fetal panel. All relevant genes from the 'Mucopolysaccharideosis, Gaucher, Fabry' V1.0 panel (lysosomal storage disorders) were also added to the Fetal hydrops panel as green together with genes from the literature where there is a reasonable link between the corresponding lysosomal storage disorder (LSD) and Fetal hydrops. All PEX genes from the V1.2 'Peroxisomal disorders' panel were added as green based on a link between peroxisomal biogenesis disorders and Fetal hydrops.

21 Dec 2016, Gel status: 0

Created

Rebecca Foulger (Genomics England curator)

HADHA was created by rfoulger

21 Dec 2016, Gel status: 0

Added New Source

Rebecca Foulger (Genomics England curator)

HADHA was added to Fetal hydropspanel. Sources: Literature