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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
adiposis dolorosa 
benign soft tissue neoplasm +   
central nervous system mesenchymal non-meningothelial tumor +  
cerebrotendinous xanthomatosis 
CLOVES syndrome 
congenital epulis 
Desmoid-type fibromatosis +  
encephalocraniocutaneous lipomatosis 
familial angiolipomatosis 
familial multiple lipomatosis 
fibrodysplasia ossificans progressiva 
fibroma +   
fibromatosis +   
fibromyxoid tumor +  
fibrosarcoma +  
FLOTCH syndrome 
glomus tumor +  
hemangioma of subcutaneous tissue  
inflammatory myofibroblastic tumor +  
isolated anhidrosis with normal sweat glands 
juvenile hyaline fibromatosis 
kaposiform hemangioendothelioma 
Lipedema 
malignant soft tissue neoplasm +  
Mazabraud syndrome 
mediastinal mesenchymal tumor +  
mixed endometrial stromal and smooth muscle tumor +  
multiple symmetric lipomatosis 
myofibroblastoma +  
nodular fasciitis 
A self-limiting, rapidly growing, non-encapsulated benign neoplasm that arises from the soft tissues. It is characterized by the presence of plump spindle-shaped fibroblasts, multinucleated osteoclast-like giant cells, chronic inflammatory infiltrate, red blood cell extravasation, and high mitotic activity.
nodular nonsuppurative panniculitis 
PEComa +   
Pierpont syndrome 
primary lipodystrophy 
Roch-Leri mesosomatous lipomatosis 
soft tissue amyloid neoplasm 
solitary fibrous tumor +  
synovium neoplasm +  

Synonyms
Exact Synonyms: DOID:7327 ;   NCIT:C3827 ;   Orphanet:477742 ;   http://identifiers.org/medgen/96076 ;   http://identifiers.org/snomedct/400138001 ;   http://linkedlifedata.com/resource/umls/id/C0410005 ;   http://purl.bioontology.org/ontology/ICD10CM/M72.4 ;   http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/789101380 ;   pseudosarcomatous fasciitis ;   pseudosarcomatous fibromatosis
Alternate IDs: MONDO:0004187
Xrefs: DOID:7327 ;   GARD:21959 ;   ICD10CM:M72.4 ;   ICD9:728.79 ;   MEDGEN:96076 ;   NCI:C3827 ;   ORDO:477742 ;   SCTID:400138001 ;   UMLS:C0410005 ;   icd11.foundation:789101380
Definition Sources: NCIT:C3827

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