Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		0.100 GeneticVariation CLINVAR Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations. 19770472

2009
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		0.100 GeneticVariation CLINVAR ASPM is a major determinant of cerebral cortical size. 12355089

2002
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		0.100 Biomarker HPO