DiseaseID 26437
卡穆拉蒂-恩格尔曼病
Camurati-Engelmann Disease
Camurati-Englemann disease (CED) is a rare, clinically variable bone dysplasia syndrome characterized by hyperostosis of the long bones, skull, spine and pelvis, associated with severe pain in the ext
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Disease: 1Symptom: 12Target: 17Links: 36
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26437
- Core Entity Id
- 119005
- Source Entity Count
- 1
- Preferred Name
- Camurati-Engelmann Disease
- Name Cn
- 卡穆拉蒂-恩格尔曼病
- Name Pinyin
- Ka Mu La Di - En Ge Er Man Bing
- Name En
- Camurati-Engelmann Disease
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- Camurati-Englemann disease (CED) is a rare, clinically variable bone dysplasia syndrome characterized by hyperostosis of the long bones, skull, spine and pelvis, associated with severe pain in the ext
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Camurati-Engelmann Disease
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C0011989C2931842
Sym Map
SMDE03448
Orphanet
1328
Etcm Disease
Camurati-Engelmann Disease
Itcmdb Generated
ITX-DISEASE-EECB4C348A32
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Camurati-Engelmann Disease Details page
Basic Information
Disease Name
Camurati-Engelmann Disease
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Bone diseases
Disease Definition
Camurati-Englemann disease (CED) is a rare, clinically variable bone dysplasia syndrome characterized by hyperostosis of the long bones, skull, spine and pelvis, associated with severe pain in the ext