acromesomelic dysplasia Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An osteochondrodysplasia that has_material_basis_in mesomelia and acromelia, which results_in short limb Dwarfism. (Human Disease Ontology, DOID_0080049)
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13 genes co-occuring with the disease acromesomelic dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
NPR2 natriuretic peptide receptor 2 3.20743
NPPC natriuretic peptide C 2.2298
OSTN osteocrin 1.63187
GDF5 growth differentiation factor 5 1.4057
NPTXR neuronal pentraxin receptor 1.33065
STOML2 stomatin (EPB72)-like 2 1.29833
STOM stomatin 0.994017
NPR3 natriuretic peptide receptor 3 0.952856
VSX2 visual system homeobox 2 0.933727
MAPK1 mitogen-activated protein kinase 1 0.626888
NPPA natriuretic peptide A 0.461639
NPR1 natriuretic peptide receptor 1 0.448441
IGF1 insulin-like growth factor 1 (somatomedin C) 0.218715