Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4538788
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE 		0.400 Biomarker disease GENOMICS_ENGLAND Frequency of CNKSR2 mutation in the X-linked epilepsy-aphasia spectrum. 28098945 2017
CUI: C4538788
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE 		0.400 CausalMutation disease CLINVAR