MID2, midline 2, 11043

N. diseases: 48; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3890168
Disease: MENTAL RETARDATION, X-LINKED 101
MENTAL RETARDATION, X-LINKED 101
0.600 GeneticVariation disease UNIPROT Targeted deep resequencing identifies MID2 mutation for X-linked intellectual disability with varied disease severity in a large kindred from India. 24115387 2014
CUI: C3890168
Disease: MENTAL RETARDATION, X-LINKED 101
MENTAL RETARDATION, X-LINKED 101
0.600 Biomarker disease CTD_human
CUI: C3890168
Disease: MENTAL RETARDATION, X-LINKED 101
MENTAL RETARDATION, X-LINKED 101
0.600 CausalMutation disease CLINVAR