NODAL, nodal growth differentiation factor, 4838

N. diseases: 89; N. variants: 12
Disease: Alobar Holoprosencephaly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0431363
Disease: Alobar Holoprosencephaly
Alobar Holoprosencephaly 		0.500 Biomarker disease CTD_human NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos. 23264560 2013
CUI: C0431363
Disease: Alobar Holoprosencephaly
Alobar Holoprosencephaly 		0.500 GermlineCausalMutation disease ORPHANET