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HADHA

—Hydroxyacyl-CoA Dehydrogenase Trifunctional Multienzyme Complex Subunit Alpha

Chromosome: 2

Location: 2:26189833-26245044

OMIM: 600890

Ensembl: ENSG00000084754

Official·OMIM:600890 Official·ENSG00000084754

Encodes mitochondrial trifunctional protein alpha subunit. Mutations cause LCHAD deficiency.

Treatment Roadmap — HADHA

Preclinical

Phase 1

Phase 2

Phase 3

Approved

Clinical trials have approximately 10% success rate. This roadmap shows the current status, not guaranteed outcomes.

Associated Diseases

Long-Chain 3-Hydroxy Acyl-CoA Dehydrogenase Deficiency

Autosomal RecessivePrevalence: 1/250000metabolic

Official·OMIM:609016 Official·ORPHA5

Summary

Clinical Trial

Approved Therapy

Registered Variant