Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3188
Gene Symbol: HNRNPH2
HNRNPH2
CUI: C4310814
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE 		0.700 Biomarker GENOMICS_ENGLAND Variants in HNRNPH2 on the X Chromosome Are Associated with a Neurodevelopmental Disorder in Females. 27545675

2016
Entrez Id: 3188
Gene Symbol: HNRNPH2
HNRNPH2
CUI: C4310814
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE 		0.700 GeneticVariation UNIPROT Variants in HNRNPH2 on the X Chromosome Are Associated with a Neurodevelopmental Disorder in Females. 27545675

2016
Entrez Id: 3188
Gene Symbol: HNRNPH2
HNRNPH2
CUI: C4310814
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE 		0.700 Biomarker CTD_human