Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2737
Gene Symbol: GLI3
GLI3 		0.500 GermlineCausalMutation disease ORPHANET Nosology and classification of genetic skeletal disorders: 2015 revision. 26394607 2015
Entrez Id: 2737
Gene Symbol: GLI3
GLI3 		0.500 GermlineCausalMutation disease ORPHANET Nonsense-mediated decay and the molecular pathogenesis of mutations in SALL1 and GLI3. 18000979 2007
Entrez Id: 2737
Gene Symbol: GLI3
GLI3 		0.500 Biomarker disease CTD_human
Entrez Id: 137392
Gene Symbol: FAM92A
FAM92A 		0.300 Biomarker disease CTD_human FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Humans and an Abnormal Limb and Digit Skeletal Phenotype in Mice. 30395363 2019
Entrez Id: 894
Gene Symbol: CCND2
CCND2 		0.300 Biomarker disease CTD_human A Novel CCND2 Mutation in a Previously Reported Case of Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and Hydrocephalus. 29642246 2018