acromesomelic dysplasia, maroteaux type Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An acromesomelic dysplasia that has_material_basis_in mutation in NPR-B receptor which results_in severe dwarfism, abnormalities of the located_in vertebral column and shortening of middle and distal segments in the located_in limb. (Human Disease Ontology, DOID_0080050)
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5 genes co-occuring with the disease acromesomelic dysplasia, maroteaux type 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 2.93539
NPPC natriuretic peptide C 1.3904
NPTXR neuronal pentraxin receptor 1.21652
MAPK1 mitogen-activated protein kinase 1 0.890488
IGF1 insulin-like growth factor 1 (somatomedin C) 0.455978