A benign, multifocal, nodular and well-circumscribed neoplasm usually seen as a congenital neoplasm or in the first year of life. It is characterized by a biphasic growth pattern and is composed of small, undifferentiated mesenchymal cells associated with branching thin-walled vessels and more mature neoplastic spindle cells with abundant eosinophilic cytoplasm in a collagenous stroma. [ NCIT:C3742 ]

This is just here as a test because I lose it

Term information

database cross reference
  • DOID:0080109 (MONDO:equivalentTo)
  • Orphanet:2591 (MONDO:equivalentTo)
  • OMIMPS:228550 (MONDO:equivalentTo)
  • ONCOTREE:IMS (MONDO:equivalentTo)
  • UMLS:C0206648 (NCIT:C3742)
  • MESH:D018224 (MONDO:equivalentTo)
  • GARD:0002998 (MONDO:equivalentTo)
  • ICDO:8824/1 (NCIT:C3742)
  • NCIT:C3742 (MONDO:equivalentTo)
  • ICD10:D48.1 (Orphanet:2591)
Subsets

gard_rare, ordo_disease

abbreviation
IMS [ ONCOTREE:IMS ]

definition

A benign, multifocal, nodular and well-circumscribed neoplasm usually seen as a congenital neoplasm or in the first year of life. It is characterized by a biphasic growth pattern and is composed of small, undifferentiated mesenchymal cells associated with branching thin-walled vessels and more mature neoplastic spindle cells with abundant eosinophilic cytoplasm in a collagenous stroma.

exactMatch

http://www.orpha.net/ORDO/Orphanet_2591

http://linkedlifedata.com/resource/umls/id/C0432284

http://purl.obolibrary.org/obo/DOID_0080109

http://identifiers.org/mesh/D018224

http://purl.obolibrary.org/obo/NCIT_C3742

http://linkedlifedata.com/resource/umls/id/C0206648

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0019300

has exact synonym

infantile hemangiopericytoma

multicentric myofibromatosis

myofibromatosis

infantile myofibromatosis

id

MONDO:0016824

seeAlso

https://rarediseases.info.nih.gov/diseases/2998/infantile-myofibromatosis

should conform to

http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml