DiseaseID 6274
胶质肉瘤
disease
NCI2016_NCI-GLOSS_1602D:A type of glioma (cancer of the brain that comes from glial, or supportive, cells).|NCI2016_02D:A rare histological variant of glioblastoma (WHO grade IV) characterized by a biphasic tissue patter
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Symptom: 3Target: 12Links: 15
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 6274
- Core Entity Id
- 62902
- Source Entity Count
- 1
- Preferred Name
- Gliosarcoma
- Name Cn
- 胶质肉瘤
- Name Pinyin
- Jiao Zhi Rou Liu
- Name En
- Gliosarcoma
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Neoplastic Process
- Disgenet Type
- disease
- Mesh Class
- Neoplasms
- Do Class
- disease of anatomical entity; disease of cellular proliferation
- Hpo Class
- Mesh Class Name
- Neoplasms
- Hpo Class Name
- Do Class Name
- disease of anatomical entity; disease of cellular proliferation
- Disease Definition
- NCI2016_NCI-GLOSS_1602D:A type of glioma (cancer of the brain that comes from glial, or supportive, cells).|NCI2016_02D:A rare histological variant of glioblastoma (WHO grade IV) characterized by a biphasic tissue pattern with alternating areas displaying glial and mesenchymal differentiation (WHO).|MSH2017_2016_08_12:Rare mixed tumors of the brain and rarely the spinal cord which contain malignant neuroectodermal (glial) and mesenchymal components, including spindle-shaped fibrosarcoma cells. These tumors are highly aggressive and present primarily in adults as rapidly expanding mass lesions. They may arise in tissue that has been previously irradiated. (From Br J Neurosurg 1995 Apr;9(2):171-8)
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Gliosarcoma
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS004452
Me Sh
D018316
Umls
C0206726
Sym Map
SMDE09055
Do Class
DOID:14566DOID:7
Dis Ge Net
C0206726
Umls Sty
T191
Me Sh Class
C04
Tcmbank Disease
1194
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity; disease of cellular proliferation
Disease Type
disease
Do Disease Class
disease of anatomical entity; disease of cellular proliferation
Umls Disease Type
Neoplastic Process
Disease Definition
NCI2016_NCI-GLOSS_1602D:A type of glioma (cancer of the brain that comes from glial, or supportive, cells).|NCI2016_02D:A rare histological variant of glioblastoma (WHO grade IV) characterized by a biphasic tissue pattern with alternating areas displaying glial and mesenchymal differentiation (WHO).|MSH2017_2016_08_12:Rare mixed tumors of the brain and rarely the spinal cord which contain malignant neuroectodermal (glial) and mesenchymal components, including spindle-shaped fibrosarcoma cells. These tumors are highly aggressive and present primarily in adults as rapidly expanding mass lesions. They may arise in tissue that has been previously irradiated. (From Br J Neurosurg 1995 Apr;9(2):171-8)
Me Sh Disease Class
Neoplasms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Neoplasms
Umls Semantic Type Name
Neoplastic Process