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thyroid dyshormonogenesis 5

Any familial thyroid dyshormonogenesis in which the cause of the disease is a mutation in the DUOXA2 gene.

Therapeutic area
Endocrine / Metabolic
Rarity
Unknown
Prevalence
—
MONDO
MONDO:0010137

Overview

Any familial thyroid dyshormonogenesis in which the cause of the disease is a mutation in the DUOXA2 gene.

Content last reviewed: 2026-06