A poorly circumscribed, intermediate fibrocytic neoplasm arising from the superficial soft tissues. It is characterized by the presence of spindle-shaped fibroblasts, and an infiltrative growth pattern. [ NCIT:C6814 ]
Synonyms: superficial Fibromatosis
Term information
- ICD9:729.99 (MONDO:relatedTo)
- EFO:1000556 (MONDO:equivalentTo)
- SCTID:238853007 (MONDO:equivalentTo)
- MEDGEN:140804 (MONDO:equivalentTo)
- Orphanet:199257 (MONDO:equivalentTo)
- UMLS:C0406571 (MONDO:equivalentTo)
- NCIT:C6814 (MONDO:exact-label-match)
matrix_llm__is_cancer_other, harrisons_view_connective_tissue_disorder, matrix_txgnn_grouping_cancer_or_benign_tumor, matrix_llm__is_glucose_dysfunction_other, otar, matrix_excluded, disease_grouping, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, harrisons_view_cancer_or_benign_tumor, harrisons_view_member, mondo_top_grouping_connective_tissue_disorder, ordo_group_of_disorders
http://linkedlifedata.com/resource/umls/id/C0406571
http://purl.obolibrary.org/obo/NCIT_C6814
http://identifiers.org/snomedct/238853007
http://www.ebi.ac.uk/efo/EFO_1000556
http://www.orpha.net/ORDO/Orphanet_199257
http://identifiers.org/medgen/140804