thyroid dyshormonogenesis 4
MONDO:0010136Mondo
Findings
No curated finding names thyroid dyshormonogenesis 4 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any familial thyroid dyshormonogenesis in which the cause of the disease is a mutation in the IYD gene.
Definition from the Mondo Disease Ontology (MONDO:0010136), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- IYDHGNC:21071
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
- Strong · PanelApp Australia · Autosomal recessive · 2025
Where it sits
- A kind of
Other names
6 names
Resolves to: thyroid dyshormonogenesis 4
- Also called
- familial thyroid dyshormonogenesis caused by mutation in IYDhypothyroidism, congenital, due to dyshormonogenesis, 4IYD familial thyroid dyshormonogenesisTDH4thyroid dyshormonogenesis type 4thyroid hormonogenesis, genetic defect in, 4