DiseaseID 5088
横纹肌肉瘤
disease
NCI2016_NICHD_1602D:A malignant neoplasm arising from skeletal myocytes.|NCI2016_NCI-GLOSS_1602D:Cancer that forms in the soft tissues in a type of muscle called striated muscle. Rhabdomyosarcoma can occur anywhere in th
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Disease: 1Symptom: 11Target: 12Links: 23
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 5088
- Core Entity Id
- 61534
- Source Entity Count
- 2
- Preferred Name
- Rhabdomyosarcoma
- Name Cn
- 横纹肌肉瘤
- Name Pinyin
- Heng Wen Ji Rou Liu
- Name En
- Rhabdomyosarcoma
- 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 musculature; Neoplasm
- Mesh Class Name
- Neoplasms
- Hpo Class Name
- Neoplasm; Abnormality of the musculature
- Do Class Name
- disease of anatomical entity; disease of cellular proliferation
- Disease Definition
- NCI2016_NICHD_1602D:A malignant neoplasm arising from skeletal myocytes.|NCI2016_NCI-GLOSS_1602D:Cancer that forms in the soft tissues in a type of muscle called striated muscle. Rhabdomyosarcoma can occur anywhere in the body.|NCI2016_CDISC_1602D:A malignant mesenchymal neoplasm arising from skeletal muscle.|NCI2016_02D:A rare aggressive malignant mesenchymal neoplasm arising from skeletal muscle. It usually occurs in children and young adults. Only a small percentage of tumors arise in the skeletal muscle of the extremities. The majority arise in other anatomical sites.|MSH2017_2016_08_12:A malignant solid tumor arising from mesenchymal tissues which normally differentiate to form striated muscle. It can occur in a wide variety of sites. It is divided into four distinct types: pleomorphic, predominantly in male adults; alveolar (RHABDOMYOSARCOMA, ALVEOLAR), mainly in adolescents and young adults; embryonal (RHABDOMYOSARCOMA, EMBRYONAL), predominantly in infants and children; and botryoidal, also in young children. It is one of the most frequently occurring soft tissue sarcomas and the most common in children under 15. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p2186; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1647-9)|CSP2006:highly malignant tumor of striated muscle derived from primitive mesenchymal cells and exhibiting differentiation along rhabdomyoblastic lines.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Rhabdomyosarcoma
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0002859
Herb
HBDIS002634
Me Sh
D012208
Umls
C0035412
Sym Map
SMDE12872
Do Class
DOID:14566DOID:7
Dis Ge Net
C0035412
Umls Sty
T191
Hpo Class
HP:0002664HP:0002664;HP:0003011HP:0003011
Me Sh Class
C04
Tcmbank Disease
256222758
Itcmdb Generated
ITX-DISEASE-1A3AF4965E5A
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 musculature
Do Disease Class
disease of anatomical entity; disease of cellular proliferation
Hpo Disease Class
Abnormality of the musculature; Neoplasm
Umls Disease Type
Neoplastic Process
Disease Definition
NCI2016_NICHD_1602D:A malignant neoplasm arising from skeletal myocytes.|NCI2016_NCI-GLOSS_1602D:Cancer that forms in the soft tissues in a type of muscle called striated muscle. Rhabdomyosarcoma can occur anywhere in the body.|NCI2016_CDISC_1602D:A malignant mesenchymal neoplasm arising from skeletal muscle.|NCI2016_02D:A rare aggressive malignant mesenchymal neoplasm arising from skeletal muscle. It usually occurs in children and young adults. Only a small percentage of tumors arise in the skeletal muscle of the extremities. The majority arise in other anatomical sites.|MSH2017_2016_08_12:A malignant solid tumor arising from mesenchymal tissues which normally differentiate to form striated muscle. It can occur in a wide variety of sites. It is divided into four distinct types: pleomorphic, predominantly in male adults; alveolar (RHABDOMYOSARCOMA, ALVEOLAR), mainly in adolescents and young adults; embryonal (RHABDOMYOSARCOMA, EMBRYONAL), predominantly in infants and children; and botryoidal, also in young children. It is one of the most frequently occurring soft tissue sarcomas and the most common in children under 15. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p2186; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1647-9)|CSP2006:highly malignant tumor of striated muscle derived from primitive mesenchymal cells and exhibiting differentiation along rhabdomyoblastic lines.
Me Sh Disease Class
Neoplasms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Neoplasms
Umls Semantic Type Name
Neoplastic Process