Disease-gene associations mined from literature

Human genes for fibrodysplasia ossificans progressiva

Fibrodysplasia ossificans progressiva [DOID:13374]

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:  fibrodysplasia ossificans progressiva,  DOID:13374,  fibrodysplasia ossificans progressivas,  Stone Man Syndrome,  myositis ossificans progressiva ...

Linkouts:  OMIM