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Summary Literature (0)
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: myositis ossificans progressiva, progressive myositis ossificans, progressive ossifying myositis, Stone Man Syndrome

Xenbase Genes : acvr1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007606 - ciliated stratified columnar epithelium

MIM:
MIM:135100 - FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), connective tissue disease (is_a)