Myofibromatosis, infantile, 1

Definition

Any myofibromatosis in which the cause of the disease is a mutation in the PDGFRB gene.

Also known as myofibromatosis caused by mutation in PDGFRB, myofibromatosis, infantile, 1, myofibromatosis, infantile, type 1, PDGFRB myofibromatosis — per MONDO

Also identified as

• DOID 0070666 per MONDO
• ICD9 756.9 per MONDO
• MESH C562978 per MONDO
• NCIT C176943 per MONDO
• OMIM 228550 per MONDO
• SCTID 254146000 per MONDO
• UMLS C4551572 per MONDO