Term Name: infantile myofibromatosis 2
Synonyms:
Definition: An infantile myofibromatosis that has_material_basis_in heterozygous mutation in the NOTCH3 gene on chromosome 19p13.
Ontology: Human Disease [DOID:0070667]   ( DOID:0070667 )

Relationships
is a type of: autosomal dominant disease infantile myofibromatosis