Disease Term Disease ID Gene Symbol Classification References Source
Mild Mental Retardation C0026106 WASHC4 Causal Pathogenic evidence from ClinVar - ClinVar
ZMYND11 Causal Pathogenic evidence from ClinVar - ClinVar
AASS Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ABCC9 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ACAT1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ACOX2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
Moderate intellectual disability C0026351 WASHC4 Causal Pathogenic evidence from ClinVar - ClinVar
ZBTB18 Causal Pathogenic evidence from ClinVar - ClinVar
ZMYND11 Causal Pathogenic evidence from ClinVar - ClinVar
ZNF711 Causal Pathogenic evidence from ClinVar 19377476, 27993705 ClinVar
Severe intellectual disability C0036857 WASHC4 Causal Pathogenic evidence from ClinVar - ClinVar
WIPI2 Causal Pathogenic evidence from ClinVar - ClinVar
ZEB2 Causal Pathogenic evidence from ClinVar - ClinVar
ZNF711 Causal Pathogenic evidence from ClinVar - ClinVar
ABCC8 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ACAT1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ACO2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ACOX1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
Intellectual Disability C3714756 WDR26 Causal Pathogenic evidence from ClinVar 28921851 ClinVar
ZBTB18 Causal Pathogenic evidence from ClinVar - ClinVar
ZBTB20 Causal Pathogenic evidence from ClinVar - ClinVar
ZDHHC9 Causal Pathogenic evidence from ClinVar 29681091 ClinVar
ZMYND11 Causal Pathogenic evidence from ClinVar 25281490, 27626064 ClinVar
ZNF148 Causal Pathogenic evidence from ClinVar - ClinVar
ZNF292 Causal Pathogenic evidence from ClinVar 29904178 ClinVar
ZNF711 Causal Pathogenic evidence from ClinVar - ClinVar
AAAS Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
AARS1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
AASS Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 27604308 -
ABCA4 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ABCA7 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ABCC8 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ABCC9 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ABHD5 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ACAT1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ACBD6 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 21937992 -
ACD Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ACE2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 26350204 -
ACER3 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ACIN1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 26350204 -
ACOT9 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 26350204 -
ACTA1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ACTA2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
MENTAL RETARDATION, AUTOSOMAL DOMINANT 22 C3808184 ZBTB18 Causal Pathogenic evidence from ClinVar 25529582, 26740508 ClinVar
MENTAL RETARDATION, AUTOSOMAL DOMINANT 30 C4015167 ZMYND11 Causal Pathogenic evidence from ClinVar 25217958 ClinVar
Mental Retardation, X-Linked C1136249 ZNF711 Causal Pathogenic evidence from ClinVar 19377476 ClinVar
Mental Retardation, X-Linked Nonsyndromic C3501611 ZNF711 Causal Pathogenic evidence from ClinVar 19377476, 21384559, 27993705, 28630650 ClinVar
Mental Retardation, X-Linked, Znf711-Related C2749020 ZNF711 Causal Pathogenic evidence from ClinVar 19377476, 27993705 ClinVar
Mental deficiency C0917816 ACBD6 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 21937992 -
Profound Mental Retardation C0020796 ACBD6 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 21937992 -