Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51114
Gene Symbol: ZDHHC9
ZDHHC9
CUI: C3275406
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE 		0.900 GeneticVariation CLINVAR

Entrez Id: 51114
Gene Symbol: ZDHHC9
ZDHHC9
CUI: C3275406
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE 		0.900 CausalMutation CLINVAR

Entrez Id: 51114
Gene Symbol: ZDHHC9
ZDHHC9
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation CLINVAR Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability. 26350204

2015
Entrez Id: 51114
Gene Symbol: ZDHHC9
ZDHHC9
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation CLINVAR Next-generation sequencing in X-linked intellectual disability. 25649377

2015
Entrez Id: 51114
Gene Symbol: ZDHHC9
ZDHHC9
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation CLINVAR Expanding the clinical phenotype of patients with a ZDHHC9 mutation. 24357419

2014
Entrez Id: 51114
Gene Symbol: ZDHHC9
ZDHHC9
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation CLINVAR A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476

2009
Entrez Id: 51114
Gene Symbol: ZDHHC9
ZDHHC9
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation CLINVAR Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus. 17436253

2007