Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Hypothyroidism, Congenital, Nongoitrous, 1 TSHR disease C3493776 Biomarker 0.8 disgenet
Hypothyroidism, Congenital, Nongoitrous, 1 TSHR disease C3493776 GermlineCausalMutation 0.8 disgenet
Hypothyroidism, Congenital, Nongoitrous, 1 TSHR disease C3493776 CausalMutation 0.8 disgenet
Hypothyroidism, Congenital, Nongoitrous, 1 TSHR disease C3493776 GeneticVariation 0.8 disgenet
Hypothyroidism, Congenital, Nongoitrous, 1 IFIH1 disease C3493776 GeneticVariation 0.1 disgenet
Hypothyroidism, Congenital, Nongoitrous, 1 CEP128 disease C3493776 CausalMutation 0.1 disgenet
Hypothyroidism, Congenital, Nongoitrous, 1 PTH disease C3493776 GeneticVariation 0.09 disgenet
Hypothyroidism, Congenital, Nongoitrous, 1 PTH disease C3493776 Biomarker 0.09 disgenet
Hypothyroidism, Congenital, Nongoitrous, 1 GNAS disease C3493776 GeneticVariation 0.03 disgenet
Hypothyroidism, Congenital, Nongoitrous, 1 SLC5A5 disease C3493776 Biomarker 0.01 disgenet
Hypothyroidism, Congenital, Nongoitrous, 1 TG disease C3493776 Biomarker 0.01 disgenet
Hypothyroidism, Congenital, Nongoitrous, 1 CHNG3 disease C3493776 Biomarker 0.01 disgenet
Hypothyroidism, Congenital, Nongoitrous, 1 DUOX2 disease C3493776 GeneticVariation 0.01 disgenet
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