Disease: Hypothyroidism ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.110 GeneticVariation disease BEFREE We suggest that hypogonadism, GH deficiency, and hypothyroidism could be possible endocrinological defects in patients with CHD7 mutations and that olfactory bulb hypoplasia as well as semicircular canal aplasia should be considered as a major sign for CHARGE syndrome and recommend a computed tomography scan of the temporal bone and magnetic resonance imaging study of the olfactory bulb region. 18089695 2008
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.110 CausalMutation disease CLINVAR
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.110 Biomarker disease HPO