Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0220998
Disease: Hypothalamic hypothyroidism
Hypothalamic hypothyroidism
0.410 GeneticVariation disease ORPHANET Isolated idiopathic central hypothyroidism in an adult, possibly caused by thyrotropin releasing hormone (TRH) deficiency. 20687402 2010
CUI: C0220998
Disease: Hypothalamic hypothyroidism
Hypothalamic hypothyroidism
0.410 Biomarker disease BEFREE TRH knockout mice show characteristic phenotypes of tertiary hypothyroidism, but no morphological changes in their cerebellum. 18418668 2008
CUI: C0220998
Disease: Hypothalamic hypothyroidism
Hypothalamic hypothyroidism
0.410 Biomarker disease HPO