Disease Term Disease ID Gene Symbol Classification References Source
Specific language impairment C0454651 CCDC136 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 25065397 -
FOXP2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 11586359, 12815709, 12876151, 15877281, 15983371, 16984964, 18052609, 18287060, 23918746, 24607928, 27572252 -
HLCS Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 27016271 -
INIP Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 25065397 -
LINC00588 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 27016271 -
RBFOX2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 25065397 -
NON RARE IN EUROPE: Specific language impairment 458713 NFXL1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
SPECIFIC LANGUAGE IMPAIRMENT 5 C3809483 NOP9 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 24571439 -
TM4SF20 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 23810381 -