Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation
0.600 GeneticVariation disease UNIPROT Mutations of the RET-GDNF signaling pathway in Ondine's curse. 9497256 1998
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation
0.600 Biomarker disease CTD_human Mutations of the RET-GDNF signaling pathway in Ondine's curse. 9497256 1998
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation
0.600 GeneticVariation disease ORPHANET
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation
0.600 Biomarker disease GENOMICS_ENGLAND