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Diseases

Brody myopathy

brody myopathy

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
Brody myopathy
Standard Disease Name
brody myopathy
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
No data
OMIM ID
No data
UMLS ID
C0334586
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:An astrocytic tumor with a relatively favorable prognosis (WHO grade II), typically encountered in children and young adults. It has a superficial location in the cerebral hemispheres and involvement of the meninges. Characteristic features include pleomorphic and lipidized cells expressing GFAP and often surrounded by a reticulin network as well as eosinophilic granular bodies. For lesions with significant mitotic activity (5 or more mitoses per 10 HPF) and/or with areas of necrosis, the designation "pleomorphic xanthoastrocytoma with anaplastic features" may be used. (WHO)
Related

Direct relations and traceable candidates grouped by relation type.

Candidate Herbs

target disease -> ingredient target -> herb ingredient8 Herbs