Search Ontology:
Human Disease

infantile myofibromatosis 1

Term ID
DOID:0070666
Synonyms
Definition
An infantile myofibromatosis that has_material_basis_in heterozygous mutation in the PDGFRB gene on chromosome 5q32. (2)
References
Ontology
Human Disease   ( DOID:0070666 )
Relationships
Other Pages
Genes Involved
Zebrafish Models
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