Search Ontology:
Human Disease

infantile myofibromatosis 2

Term ID
DOID:0070667
Synonyms
Definition
An infantile myofibromatosis that has_material_basis_in heterozygous mutation in the NOTCH3 gene on chromosome 19p13. https://pmc.ncbi.nlm.nih.gov/articles/PMC3675260/
References
Ontology
Human Disease   ( DOID:0070667 )
Relationships
Other Pages
Genes Involved
Zebrafish Models
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