Thyroid agenesis

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL ABSENCE OF THYROID GLAND
C0749420
IGSF1 Unknown — Disgenet
NKX2-5 Unknown — Disgenet
PAX8 Unknown — Disgenet
SLC26A4 Unknown — Disgenet
THRA Unknown — Disgenet
TSHB Unknown — Disgenet
TSHR Unknown — Disgenet
All7 Causal0 Unknown7
Related Diseases Diseases that share the most curated genes with Thyroid agenesis.
5 View disease cluster →
Congenital thyroid atrophy 6 shared genesTSHR, NKX2-5, THRA, PAX8, TSHB, IGSF1 Related via 6 shared genes including TSHR, NKX2-5, THRA. Congenital hypothyroidism without goiter 6 shared genesTSHR, NKX2-5, THRA, PAX8, TSHB, IGSF1 Related via 6 shared genes including TSHR, NKX2-5, THRA. Congenital hypothyroidism due to absence of thyroid gland 4 shared genesTSHR, NKX2-5, PAX8, SLC26A4 Related via 4 shared genes including TSHR, NKX2-5, PAX8. Congenital hypothyroidism 7 shared genesTSHR, NKX2-5, THRA, PAX8, SLC26A4, TSHB, IGSF1 Related via 7 shared genes including TSHR, NKX2-5, THRA. Interrupted aortic arch 1 shared geneNKX2-5 Related via 1 shared gene including NKX2-5.