Progressive myositis ossificans Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description .A connective tissue disease that is characterized by progressive ossification of skeletal muscle, fascia, tendons, and ligaments and has_material_basis_in heterozygous mutation in the ACVR1 gene. (Human Disease Ontology, DOID_13374)
External Link
Similar Terms
Downloads & Tools


1 genes associated with the Progressive myositis ossificans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
ACVR1 activin A receptor, type I