Gene: SNORD118 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 727676
Gene Symbol: SNORD118
SNORD118 		0.710 GeneticVariation disease BEFREE Leukoencephalopathy, Intracranial Calcifications, Cysts, and SNORD118 Mutation (Labrune Syndrome) with Obstructive Hydrocephalus. 30794980 2019
Entrez Id: 727676
Gene Symbol: SNORD118
SNORD118 		0.710 Biomarker disease GENOMICS_ENGLAND Identification of novel SNORD118 mutations in seven patients with leukoencephalopathy with brain calcifications and cysts. 28177126 2017
Entrez Id: 727676
Gene Symbol: SNORD118
SNORD118 		0.710 GermlineCausalMutation disease ORPHANET Identification of novel SNORD118 mutations in seven patients with leukoencephalopathy with brain calcifications and cysts. 28177126 2017
Entrez Id: 727676
Gene Symbol: SNORD118
SNORD118 		0.710 GermlineCausalMutation disease ORPHANET Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts. 27571260 2016
Entrez Id: 727676
Gene Symbol: SNORD118
SNORD118 		0.710 Biomarker disease GENOMICS_ENGLAND Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts. 27571260 2016
Entrez Id: 727676
Gene Symbol: SNORD118
SNORD118 		0.710 CausalMutation disease CLINVAR
Entrez Id: 727676
Gene Symbol: SNORD118
SNORD118 		0.710 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 727676
Gene Symbol: SNORD118
SNORD118 		0.710 Biomarker disease CTD_human