multiple epiphyseal dysplasia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An osteochondrodysplasia that has_material_basis_in defective cartilage mineralization into bone which results_in irregular ossification centers of the located_in hip or located_in knee. The disease has_symptom fatigue, has_symptom joint pain. (Human Disease Ontology, DOID_12721)
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2 genes associated with the disease multiple epiphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
MATN3 matrilin 3
MB myoglobin