Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266453
Disease: Exencephaly
Exencephaly
0.310 GeneticVariation disease BEFREE Grainyhead-like genes represent candidates for involvement in NTDs based on the presence of SB and exencephaly in mice carrying loss-of-function alleles of Grhl2 or Grhl3. 30189017 2018
CUI: C0266453
Disease: Exencephaly
Exencephaly
0.310 Biomarker disease CTD_human Differential response of heterozygous curly-tail mouse embryos to vitamin A teratogenesis depending on maternal genotype. 6635991 1983