DiseaseID 5086
横纹肌溶解症
phenotype
NCI2016_NICHD_1602D:A clinical syndrome resulting from direct or indirect muscle injury and subsequent release of myoglobin into the plasma.|NCI2016_02D:A clinical syndrome resulting from direct or indirect muscle injury
Relationship Network
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Disease: 1Symptom: 12Target: 12Links: 24
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 5086
- Core Entity Id
- 61530
- Source Entity Count
- 2
- Preferred Name
- Rhabdomyolysis
- Name Cn
- 横纹肌溶解症
- Name Pinyin
- Heng Wen Ji Rong Jie Zheng
- Name En
- Rhabdomyolysis
- Name Latin
- Bilingual Status
- complete
- Disease Type
- phenotype
- Umls Disease Type
- Pathologic Function
- Disgenet Type
- phenotype
- Mesh Class
- Musculoskeletal Diseases
- Do Class
- Hpo Class
- Abnormality of the musculature
- Mesh Class Name
- Musculoskeletal Diseases
- Hpo Class Name
- Abnormality of the musculature
- Do Class Name
- Disease Definition
- NCI2016_NICHD_1602D:A clinical syndrome resulting from direct or indirect muscle injury and subsequent release of myoglobin into the plasma.|NCI2016_02D:A clinical syndrome resulting from direct or indirect muscle injury and subsequent release of myoglobin into the plasma.|MSH2017_2016_08_12:Necrosis or disintegration of skeletal muscle often followed by myoglobinuria.|HPO2016_07_04:Breakdown of muscle fibers that leads to the release of muscle fiber contents (myoglobin) into the bloodstream. [HPO:probinson]|CHV2011_02:a potentially fatal disease that destroys skeletal muscle
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Rhabdomyolysis
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0003201
Herb
HBDIS002632
Me Sh
D012206
Umls
C0035410
Icd10
M62.82
Sym Map
SMDE12870
Dis Ge Net
C0035410
Umls Sty
T046
Hpo Class
HP:0003011
Me Sh Class
C05
Tcmbank Disease
136731544
Itcmdb Generated
ITX-DISEASE-1E889357FFFE
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
phenotype
Hpo Class Name
Abnormality of the musculature
Hpo Disease Class
Abnormality of the musculature
Umls Disease Type
Pathologic Function
Disease Definition
NCI2016_NICHD_1602D:A clinical syndrome resulting from direct or indirect muscle injury and subsequent release of myoglobin into the plasma.|NCI2016_02D:A clinical syndrome resulting from direct or indirect muscle injury and subsequent release of myoglobin into the plasma.|MSH2017_2016_08_12:Necrosis or disintegration of skeletal muscle often followed by myoglobinuria.|HPO2016_07_04:Breakdown of muscle fibers that leads to the release of muscle fiber contents (myoglobin) into the bloodstream. [HPO:probinson]|CHV2011_02:a potentially fatal disease that destroys skeletal muscle
Me Sh Disease Class
Musculoskeletal Diseases
Dis Ge Net Disease Type
phenotype
Disease Class Name Me Sh
Musculoskeletal Diseases
Umls Semantic Type Name
Pathologic Function