Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2571
Gene Symbol: GAD1
GAD1 		0.700 Biomarker disease GENOMICS_ENGLAND Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disorders. 15571623 2004
Entrez Id: 2571
Gene Symbol: GAD1
GAD1 		0.700 GeneticVariation disease UNIPROT Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disorders. 15571623 2004
Entrez Id: 2571
Gene Symbol: GAD1
GAD1 		0.700 GermlineCausalMutation disease ORPHANET Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disorders. 15571623 2004
Entrez Id: 2571
Gene Symbol: GAD1
GAD1 		0.700 GeneticVariation disease CLINVAR
Entrez Id: 2571
Gene Symbol: GAD1
GAD1 		0.700 Biomarker disease CTD_human
Entrez Id: 2571
Gene Symbol: GAD1
GAD1 		0.700 CausalMutation disease CLINVAR
Entrez Id: 120
Gene Symbol: ADD3
ADD3 		0.300 GermlineCausalMutation disease ORPHANET Mutations in γ adducin are associated with inherited cerebral palsy. 23836506 2013
Entrez Id: 23189
Gene Symbol: KANK1
KANK1 		0.300 GermlineCausalMutation disease ORPHANET Deletion of the ANKRD15 gene at 9p24.3 causes parent-of-origin-dependent inheritance of familial cerebral palsy. 16301218 2005