DiseaseID 4787
骨母细胞瘤
disease
NCI2016_CDISC_1602D:A benign neoplasm of bone, characterized by the formation of osteoid tissue and large osteoblast-like cells.|NCI2016_02D:A rare benign bone-forming neoplasm usually arising from the spine. It is a wel
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: 5Target: 11Links: 16
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4787
- Core Entity Id
- 61189
- Source Entity Count
- 1
- Preferred Name
- Osteoblastoma
- Name Cn
- 骨母细胞瘤
- Name Pinyin
- Gu Mu Xi Bao Liu
- Name En
- Osteoblastoma
- 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
- Abnormality of the skeletal system; Neoplasm
- Mesh Class Name
- Neoplasms
- Hpo Class Name
- Neoplasm; Abnormality of the skeletal system
- Do Class Name
- disease of anatomical entity; disease of cellular proliferation
- Disease Definition
- NCI2016_CDISC_1602D:A benign neoplasm of bone, characterized by the formation of osteoid tissue and large osteoblast-like cells.|NCI2016_02D:A rare benign bone-forming neoplasm usually arising from the spine. It is a well-circumscribed lytic tumor that varies in size. The tumor is composed of woven bone trabeculae and shares similar histologic characteristics with the osteoid osteoma. Surgical curettage is the treatment of choice. The prognosis is excellent.|MSH2017_2016_08_12:A benign, painful, tumor of bone characterized by the formation of osteoid tissue, primitive bone and calcified tissue. It occurs frequently in the spine of young persons. (From Dorland, 27th ed; Stedman, 25th ed)|HPO2016_07_04:A benign, painful, tumor of bone characterized by the formation of osteoid tissue, primitive bone and calcified tissue. [HPO:probinson]
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Osteoblastoma
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0011846
Herb
HBDIS002210
Me Sh
D018215
Umls
C0029417
Sym Map
SMDE11678
Do Class
DOID:14566DOID:7
Dis Ge Net
C0029417
Umls Sty
T191
Hpo Class
HP:0000924HP:0002664
Me Sh Class
C04
Tcmbank Disease
19294
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
Hpo Class Name
Neoplasm; Abnormality of the skeletal system
Do Disease Class
disease of anatomical entity; disease of cellular proliferation
Hpo Disease Class
Abnormality of the skeletal system; Neoplasm
Umls Disease Type
Neoplastic Process
Disease Definition
NCI2016_CDISC_1602D:A benign neoplasm of bone, characterized by the formation of osteoid tissue and large osteoblast-like cells.|NCI2016_02D:A rare benign bone-forming neoplasm usually arising from the spine. It is a well-circumscribed lytic tumor that varies in size. The tumor is composed of woven bone trabeculae and shares similar histologic characteristics with the osteoid osteoma. Surgical curettage is the treatment of choice. The prognosis is excellent.|MSH2017_2016_08_12:A benign, painful, tumor of bone characterized by the formation of osteoid tissue, primitive bone and calcified tissue. It occurs frequently in the spine of young persons. (From Dorland, 27th ed; Stedman, 25th ed)|HPO2016_07_04:A benign, painful, tumor of bone characterized by the formation of osteoid tissue, primitive bone and calcified tissue. [HPO:probinson]
Me Sh Disease Class
Neoplasms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Neoplasms
Umls Semantic Type Name
Neoplastic Process