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 http://www.omim.org/entry/135100
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Genes

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