GLI3, GLI family zinc finger 3, 2737

N. diseases: 400; N. variants: 73
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0265306
Disease: Greig cephalopolysyndactyly syndrome
Greig cephalopolysyndactyly syndrome 		1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C4282400
Disease: Polydactyly, Postaxial, Type A1
Polydactyly, Postaxial, Type A1 		0.710 Biomarker disease CTD_human
CUI: C4282400
Disease: Polydactyly, Postaxial, Type A1
Polydactyly, Postaxial, Type A1 		0.710 Biomarker disease GENOMICS_ENGLAND
CUI: C0152427
Disease: Polydactyly
Polydactyly 		0.700 Biomarker disease HPO
CUI: C1868111
Disease: Polydactyly, preaxial 4
Polydactyly, preaxial 4 		0.700 Biomarker disease CTD_human
CUI: C1868111
Disease: Polydactyly, preaxial 4
Polydactyly, preaxial 4 		0.700 CausalMutation disease CLINVAR
CUI: C1868111
Disease: Polydactyly, preaxial 4
Polydactyly, preaxial 4 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C0342418
Disease: Hypothalamic hamartomas
Hypothalamic hamartomas 		0.630 Biomarker disease HPO
CUI: C0342418
Disease: Hypothalamic hamartomas
Hypothalamic hamartomas 		0.630 Biomarker disease CTD_human
CUI: C3887487
Disease: Postaxial polydactyly type A
Postaxial polydactyly type A 		0.620 Biomarker disease CTD_human
CUI: C3887487
Disease: Postaxial polydactyly type A
Postaxial polydactyly type A 		0.620 Biomarker disease GENOMICS_ENGLAND
CUI: C1868120
Disease: POSTAXIAL POLYDACTYLY, TYPE B
POSTAXIAL POLYDACTYLY, TYPE B 		0.500 Biomarker disease CTD_human
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL 		0.490 GeneticVariation disease CLINVAR
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL 		0.490 Biomarker disease CTD_human
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.310 Biomarker disease HPO
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.310 GeneticVariation disease UNIPROT
CUI: C0848558
Disease: Hypospadias
Hypospadias 		0.300 Biomarker disease HPO
CUI: C0878659
Disease: Disproportionate short stature
Disproportionate short stature 		0.300 Biomarker phenotype GENOMICS_ENGLAND
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		0.160 Biomarker disease HPO
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis 		0.130 Biomarker disease HPO
CUI: C0079541
Disease: Holoprosencephaly
Holoprosencephaly 		0.120 Biomarker disease HPO
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly 		0.120 Biomarker disease HPO
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate 		0.110 Biomarker disease HPO
CUI: C0017638
Disease: Glioma
Glioma 		0.110 Biomarker disease HPO
CUI: C0078982
Disease: Arhinencephaly
Arhinencephaly 		0.110 Biomarker disease HPO