DiseaseID 3640
脊索瘤
disease
NCI2016_NCI-GLOSS_1602D:A type of bone cancer that usually starts in the lower spinal column or at the base of the skull.|NCI2016_CDISC_1602D:A malignant bone neoplasm arising from the remnants of the fetal notochord.|NC
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Disease: 1Herb: 6Symptom: 6Target: 24Links: 36
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3640
- Core Entity Id
- 59870
- Source Entity Count
- 2
- Preferred Name
- Chordoma
- Name Cn
- 脊索瘤
- Name Pinyin
- Ji Suo Liu
- Name En
- Chordoma
- 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_NCI-GLOSS_1602D:A type of bone cancer that usually starts in the lower spinal column or at the base of the skull.|NCI2016_CDISC_1602D:A malignant bone neoplasm arising from the remnants of the fetal notochord.|NCI2016_02D:A malignant bone tumor arising from the remnants of the fetal notochord. Although it can occur at all ages, it is more frequently seen in middle-aged adults. The most frequent sites of involvement are the sacrococcygeal area, spheno-occipital area, and cervico-thoraco-lumbar spine. Microscopically, chordomas are composed of cells that form cords and lobules, separated by mucoid intercellular tissue. Some of the cells are large (physaliphorous) and have vacuolated cytoplasm and prominent vesicular nuclei. Other tumor cells are small with small nuclei without visible nucleoli. Chordomas tend to recur and may metastasize. The most common sites of metastasis are the skin and bone.|MSH2017_2016_08_12:A malignant tumor arising from the embryonic remains of the notochord. It is also called chordocarcinoma, chordoepithelioma, and notochordoma. (Dorland, 27th ed)|HPO2016_07_04:A chordoma is a tumors that arises from embryonic remnants of the notochord along the length of the neuraxis. Chordomas generally occur in the sacrum, intracranially at the clivus, or along the spinal axis. [HPO:probinson]|CSP2006:malignant tumor arising from the embryonic remains of the notochord; also called chordocarcinoma, chordoepithelioma, and notochordoma.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Chordoma
Role
preferred
Name
Chdm
Role
alias
Name
Chordoma, Susceptibility To
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0010762
Herb
HBDIS000564
Me Sh
D002817
Umls
C0008487
Sym Map
SMDE07072
Do Class
DOID:14566DOID:7
Dis Ge Net
C0008487
Umls Sty
T191
Hpo Class
HP:0000924HP:0002664
Me Sh Class
C04
Etcm Disease
Chordoma
Tcmbank Disease
297479135
Itcmdb Generated
ITX-DISEASE-4885795569C2ITX-DISEASE-AFD9704FB44A
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Page Title
Disease Chordoma Details page
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
Basic Information
Disease Name
Chordoma
Global Category
Cancer diseases;Rare diseases
Anatomical Category
Bone diseases;Endocrine diseases
Disease Definition
NCI2016_NCI-GLOSS_1602D:A type of bone cancer that usually starts in the lower spinal column or at the base of the skull.|NCI2016_CDISC_1602D:A malignant bone neoplasm arising from the remnants of the fetal notochord.|NCI2016_02D:A malignant bone tumor arising from the remnants of the fetal notochord. Although it can occur at all ages, it is more frequently seen in middle-aged adults. The most frequent sites of involvement are the sacrococcygeal area, spheno-occipital area, and cervico-thoraco-lumbar spine. Microscopically, chordomas are composed of cells that form cords and lobules, separated by mucoid intercellular tissue. Some of the cells are large (physaliphorous) and have vacuolated cytoplasm and prominent vesicular nuclei. Other tumor cells are small with small nuclei without visible nucleoli. Chordomas tend to recur and may metastasize. The most common sites of metastasis are the skin and bone.|MSH2017_2016_08_12:A malignant tumor arising from the embryonic remains of the notochord. It is also called chordocarcinoma, chordoepithelioma, and notochordoma. (Dorland, 27th ed)|HPO2016_07_04:A chordoma is a tumors that arises from embryonic remnants of the notochord along the length of the neuraxis. Chordomas generally occur in the sacrum, intracranially at the clivus, or along the spinal axis. [HPO:probinson]|CSP2006:malignant tumor arising from the embryonic remains of the notochord; also called chordocarcinoma, chordoepithelioma, and notochordoma.
Me Sh Disease Class
Neoplasms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Neoplasms
Umls Semantic Type Name
Neoplastic Process