DiseaseID 31314
21三体综合征
Trisomy 21
NCI2016_02D:A chromosomal abnormality consisting of the presence of a third copy of chromosome 21 in somatic cells.
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Disease: 1Symptom: 1Target: 12Links: 13
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 31314
- Core Entity Id
- 123882
- Source Entity Count
- 1
- Preferred Name
- Trisomy 21
- Name Cn
- 21三体综合征
- Name Pinyin
- 21 San Ti Zong He Zheng
- Name En
- Trisomy 21
- 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
- NCI2016_02D:A chromosomal abnormality consisting of the presence of a third copy of chromosome 21 in somatic cells.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Trisomy 21
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C3537167
Sym Map
SMDE14015
Itcmdb Generated
ITX-DISEASE-4C50992405EE
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Definition
NCI2016_02D:A chromosomal abnormality consisting of the presence of a third copy of chromosome 21 in somatic cells.