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
IYD Unknown
20537182 21543982
Disgenet, Orphanet
SLC5A5 Unknown
20537182 21543982
Disgenet, GWAS catalog, Orphanet
TG Unknown
20537182 21543982
Disgenet, Orphanet
TPO Unknown
20537182 21543982
Disgenet, GenCC, Orphanet
THYROID DYSHORMONOGENESIS 2A
274500MESH:C563206MONDO:0010133
TPO Unknown
11061528 23236987 25564141
CTD, HPO, Orphanet
THYROID DYSHORMONOGENESIS 3
C0342194274700MESH:C562769MONDO:0010135
SLA Unknown — Disgenet —
TG Unknown
12915634 16720658 19837936 23164529 250556 251032 251482 282464
CTD, Disgenet, GWAS catalog, HPO
THYROID DYSHORMONOGENESIS 4
274800C0342195MESH:C562770MONDO:0010136
IYD Unknown
18434651 18765512 36633921
CTD, Disgenet, GWAS catalog, HPO
THYROID DYSHORMONOGENESIS 5
274900C0342196MESH:C562771MONDO:0010137
DUOXA2 Unknown
18042646 21367925 23292166 25675383 26709262 26990548 28626131
CTD, Disgenet, GWAS catalog, 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.