| Dataset | OMIM Gene-Disease 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 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the fibrodysplasia ossificans progressiva phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ACVR1 | activin A receptor, type I |
