Disease #03889 (IMF2 (myofibromatosis, infantile, type 2 (IMF-2)), OMIM:615293)

Official abbreviation IMF2
Name myofibromatosis, infantile, type 2 (IMF-2)
OMIM ID 615293
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene NOTCH3
Associated tissues -
Disease features -
Remarks -

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