Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3809039
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36 		0.700 Biomarker disease GENOMICS_ENGLAND A novel 8-bp duplication in ADAT3 causes mild intellectual disability. 29796286 2018
CUI: C3809039
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36 		0.700 Biomarker disease GENOMICS_ENGLAND A novel 8-bp duplication in ADAT3 causes mild intellectual disability. 29796286 2018
CUI: C3809039
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36 		0.700 GermlineCausalMutation disease ORPHANET Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus. 23620220 2013
CUI: C3809039
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36 		0.700 GeneticVariation disease UNIPROT Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus. 23620220 2013
CUI: C3809039
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36 		0.700 CausalMutation disease CLINVAR
CUI: C3809039
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36 		0.700 Biomarker disease CTD_human
CUI: C3809039
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36 		0.700 GeneticVariation disease CLINVAR