NKX2-1, NK2 homeobox 1, 7080

N. diseases: 319; N. variants: 20
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0749420
Disease: Thyroid Agenesis
Thyroid Agenesis
0.400 GeneticVariation disease ORPHANET Next-generation sequencing of NKX2.1, FOXE1, PAX8, NKX2.5, and TSHR in 100 Chinese patients with congenital hypothyroidism and athyreosis. 28455095 2017
CUI: C0749420
Disease: Thyroid Agenesis
Thyroid Agenesis
0.400 Biomarker disease HPO