Myofibromatosis

Preferred Label : Myofibromatosis;

NCIt synonyms : Multicentric Myofibromatosis; Infantile Hemangiopericytoma;

NCIt related terms : Infantile myofibromatosis;

NCIt 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.;

Neoplastic status : Benign;

ICD-O code : 8824/1;

Details

Origin ID

C3742;

UMLS CUI

C0206648;

Automatic exact mappings (from CISMeF team)
- Congenital generalised fibromatosis [ICD-11 Extension code]
- fibromatosis, congenital generalized [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Myofibromatosis [PASCAL descriptor]
- Myofibromatosis [HPO term]
- Myofibromatosis [ICD-11 Extension code]
- Myofibromatosis [ICD-O code]
- Myofibromatosis (morphologic abnormality) [SNOMED CT concept]
- myofibromatosis [Disease (Nov.)]
- myofibromatosis [MeSH Descriptor]
- myofibromatosis [MeSH concept]
- myofibromatosis [SNOMED Notion]
Disease excludes abnormal cell
- Malignant Cell [NCIt concept]
Disease excludes normal cell origin
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
Disease may have findings
- Hyalinized Stroma Formation [NCIt concept]
- Necrotic Change [NCIt concept]
Has associated anatomic sites
- Connective and Soft Tissue [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Myofibromatosis [ICD-O code]
- Myofibromatosis [PASCAL descriptor]
- Myofibromatosis [HPO term]
- Myofibromatosis (disorder) [SNOMED CT concept]
- Myofibromatosis (morphologic abnormality) [SNOMED CT concept]
- myofibromatosis [Disease (Nov.)]
- myofibromatosis [MeSH concept]
- myofibromatosis [SNOMED Notion]
- myofibromatosis [MeSH Descriptor]
Validated automatic mappings to BTNT
- Infantile myofibromatosis [PASCAL descriptor]
- Infantile myofibromatosis [ORDO Disease]
- Infantile myofibromatosis [OMIM phenotypic series]
- Infantile myofibromatosis (disorder) [SNOMED CT concept]
- infantile myofibromatosis [DO Concept]
- infantile myofibromatosis [Radlex concept]
concept_is_in_subset
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology Terminology [NCIt concept]
- Mapped ICDO3.1 Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology Terminology [NCIt concept]
- Mapped ICDO3.2 Terminology [NCIt concept]
disease_excludes_finding
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Connective and Soft Tissue Cell [NCIt concept]
- Neoplastic Spindle Cell [NCIt concept]
disease_has_finding
- Benign Cellular Infiltrate [NCIt concept]
- Biphasic Pattern [NCIt concept]
- Indolent Clinical Course [NCIt concept]
- Multifocal Lesion [NCIt concept]
- Perivascular Arrangement of Tumor Cells [NCIt concept]
disease_has_normal_cell_origin
- Connective and Soft Tissue Cell [NCIt concept]
- Pericyte [NCIt concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
- Soft Tissue [NCIt concept]
related_to_genetic_biomarker
- NOTCH3 Gene [NCIt concept]
- PDGFRB Gene [NCIt concept]

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