hypochondroplasia Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An osteochondrodysplasia that has_material_basis_in mutation in the FGFR3 gene which affects ossification of cartilage and results_in short limb dwarfism. (Human Disease Ontology, DOID_0080041)
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Genes

28 genes co-occuring with the disease hypochondroplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
FGFR3 fibroblast growth factor receptor 3 2.99005
FGFR2 fibroblast growth factor receptor 2 1.47725
TK1 thymidine kinase 1, soluble 1.44869
SHOX short stature homeobox 1.29265
FGF3 fibroblast growth factor 3 1.16264
RASIP1 Ras interacting protein 1 1.02608
ATF2 activating transcription factor 2 0.950769
FGF13 fibroblast growth factor 13 0.926692
COMP cartilage oligomeric matrix protein 0.826178
STAT1 signal transducer and activator of transcription 1, 91kDa 0.81018
FGF17 fibroblast growth factor 17 0.808949
FGFR1 fibroblast growth factor receptor 1 0.754527
FGF1 fibroblast growth factor 1 (acidic) 0.707961
ARID1B AT rich interactive domain 1B (SWI1-like) 0.648138
COL10A1 collagen, type X, alpha 1 0.624143
COL2A1 collagen, type II, alpha 1 0.588222
SLC26A2 solute carrier family 26 (anion exchanger), member 2 0.53928
PTH1R parathyroid hormone 1 receptor 0.428891
STAT5B signal transducer and activator of transcription 5B 0.382223
NPPC natriuretic peptide C 0.378514
STAT5A signal transducer and activator of transcription 5A 0.372587
FGF4 fibroblast growth factor 4 0.326646
CREB1 cAMP responsive element binding protein 1 0.318272
IGF1 insulin-like growth factor 1 (somatomedin C) 0.274376
TRIM37 tripartite motif containing 37 0.190168
PPT1 palmitoyl-protein thioesterase 1 0.188938
FOXM1 forkhead box M1 0.185612
JAK1 Janus kinase 1 0.178682