Disease Term Disease ID Gene Symbol Classification References Source
PARIETAL FORAMINA C1868598 ALX4 Causal Pathogenic evidence from ClinVar 16319823, 29215649 ClinVar
MSX2 Causal Pathogenic evidence from ClinVar 16319823 ClinVar
ALX1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ALX3 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
CREBBP Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
EP300 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
EXT2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
FGFR2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
PHF21A Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
RPS19 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
TWIST1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
PARIETAL FORAMINA 2 C1865044 ALX4 Causal Pathogenic evidence from ClinVar 11106354, 11137991, 29215649 ClinVar
PARIETAL FORAMINA 1 C1868599 MSX2 Causal Pathogenic evidence from ClinVar 10742103, 10767351, 23918290 ClinVar