Thyroid dyshormonogenesis

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
FAMILIAL THYROID DYSHORMONOGENESIS
95716C4273748MONDO:0010132
DUOX2 Causal
20537182 21543982
Disgenet, Orphanet
DUOXA2 Causal
20537182 21543982
Disgenet, GWAS catalog, Orphanet
THYROID DYSHORMONOGENESIS 1
274400C1848805MESH:C564766MONDO:0020716
SLC5A5 Causal
9745458 3998954 9171822 9388506 3451231 9486973
CTD, ClinVar, Disgenet, GWAS catalog, HPO
THYROID DYSHORMONOGENESIS 6
607200C1846632MESH:C564608MONDO:0011792
DUOX2 Causal — CTD, ClinVar, Disgenet, GenCC, HPO
All7 Causal3 Unknown6
Related Diseases Diseases that share the most curated genes with Thyroid dyshormonogenesis.
5 View disease cluster →
Congenital hypothyroidism 5 shared genesIYD, TPO, SLC5A5, DUOX2, DUOXA2 Related via 5 shared genes including IYD, TPO, SLC5A5. Iodide peroxidase deficiency 1 shared geneTPO Related via 1 shared gene including TPO. Genetic transient congenital hypothyroidism 1 shared geneDUOX2 Related via 1 shared gene including DUOX2. Testicular hydrocele 2 shared genesTG, SLA Related via 2 shared genes including TG, SLA. Dwarfism 1 shared geneTG Related via 1 shared gene including TG.