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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.

Related Targets

target disease8 Targets
01
ATP2A1
ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 1
ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 1
02
ATP2A2
ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2
ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2
03
CAMP
cathelicidin antimicrobial peptide
cathelicidin antimicrobial peptide
05
CYP24A1
cytochrome P450 family 24 subfamily A member 1
cytochrome P450 family 24 subfamily A member 1
07
MSR1
macrophage scavenger receptor 1
macrophage scavenger receptor 1