CRBN, cereblon, 51185

N. diseases: 130; N. variants: 16
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3151462
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14 		0.200 Biomarker disease MGD Rescue of Learning and Memory Deficits in the Human Nonsyndromic Intellectual Disability Cereblon Knock-Out Mouse Model by Targeting the AMP-Activated Protein Kinase-mTORC1 Translational Pathway. 29459374 2018
CUI: C3151462
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14 		0.200 Biomarker disease MGD Behavioral characterization of cereblon forebrain-specific conditional null mice: a model for human non-syndromic intellectual disability. 21995942 2012