achondrogenesis Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An osteochondrodysplasia that has_material_basis_in deficient endochondral ossification which results_in dwarfism, short-trunk, short-limbed, anascara, disaprportionately large cranium, and a narrow chest which leads to death in utero or during early neonatal period. (Human Disease Ontology, DOID_0080043)
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Genes

2 genes involed in the disease achondrogenesis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
COL2A1 collagen, type II, alpha 1
SLC26A2 solute carrier family 26 (anion exchanger), member 2