Disease #03889 (IMF-2 (myofibromatosis, infantile, type 2 (IMF-2)), OMIM:615293)

Official abbreviation IMF-2
Name myofibromatosis, infantile, type 2 (IMF-2)
OMIM ID 615293
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NOTCH3
Associated tissues -
Disease features -
Remarks -