| Gene | Score gda | Association Type | Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.930 | Biomarker | disease | MGD | FGF and EDA pathways control initiation and branching of distinct subsets of developing nasal glands. | 27590203 | 2016 | ||||
|
0.930 | GeneticVariation | disease | BEFREE | Moreover, haploinsufficiency caused by defective FGF10 mutants leads to LADD syndrome. | 17682060 | 2007 | ||||
|
0.930 | GeneticVariation | disease | BEFREE | Mutations in fibroblast growth factor receptor 2 (FGFR2) and its ligand, FGF10, are known to cause lacrimo-auriculo-dento-digital (LADD) syndrome. | 18056630 | 2007 | ||||
|
0.930 | GeneticVariation | disease | UNIPROT | We conclude that ALSG and LADD syndrome may represent variable presentations of the same clinical spectrum caused by FGF10 mutations. | 16630169 | 2006 | ||||
|
0.930 | Biomarker | disease | GENOMICS_ENGLAND | We conclude that ALSG and LADD syndrome may represent variable presentations of the same clinical spectrum caused by FGF10 mutations. | 16630169 | 2006 | ||||
|
0.930 | GeneticVariation | disease | UNIPROT | Mutations in different components of FGF signaling in LADD syndrome. | 16501574 | 2006 | ||||
|
0.930 | GermlineCausalMutation | disease | ORPHANET | We conclude that ALSG and LADD syndrome may represent variable presentations of the same clinical spectrum caused by FGF10 mutations. | 16630169 | 2006 | ||||
|
0.930 | GeneticVariation | disease | BEFREE | We conclude that ALSG and LADD syndrome may represent variable presentations of the same clinical spectrum caused by FGF10 mutations. | 16630169 | 2006 | ||||
|
0.930 | Biomarker | disease | GENOMICS_ENGLAND | Morphogenesis. | 9988217 | 1999 | ||||
|
0.930 | Biomarker | disease | CTD_human | |||||||
|
0.930 | Biomarker | disease | GENOMICS_ENGLAND | |||||||
|
0.930 | GeneticVariation | disease | CLINVAR | |||||||
|
0.930 | CausalMutation | disease | CLINVAR |