Disease: Respiratory Depression ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0235063
Disease: Respiratory Depression
Respiratory Depression 		0.300 Biomarker phenotype CTD_human Severe respiratory phenotype caused by a de novo Arg528Gly mutation in the CACNA1S gene in a patient with hypokalemic periodic paralysis. 19822448 2010