Skip to main content
Diseases

Myofibromatosis

myofibromatosis

Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Myofibromatosis
Standard Disease Name
myofibromatosis
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D018224
OMIM ID
MTHU043892
UMLS ID
C0206648
HPO ID
No data

Description and Extensions

Description
NCI2016_02D: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.|MSH2017_2016_08_12:A condition characterized by multiple formations of myofibromas (LEIOMYOMA).