Term Name: infantile myofibromatosis 1
Synonyms:
Definition: An infantile myofibromatosis that has_material_basis_in heterozygous mutation in the PDGFRB gene on chromosome 5q32.
Ontology: Human Disease [DOID:0070666]   ( DOID:0070666 )

Relationships
is a type of: autosomal dominant disease infantile myofibromatosis