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DOID:13374 - fibrodysplasia ossificans progressiva
Disease Ontology Definition:.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.
Synonyms: Stone Man Syndrome, myositis ossificans progressiva, progressive myositis ossificans, progressive ossifying myositis,
Echinobase Genes
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| MIM:135100 - fibrodysplasia ossificans progressiva; fop |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
connective tissue disease (is_a)