DiseaseID 27817
染色体重复
Chromosomal Duplication
NCI2016_02D:An irregularity in the number of chromosomes, usually in the form of a gain of genetic material. (NCI)|MSH2017_2016_08_12:An aberration in which an extra chromosome or a chromosomal segment is made.
Relationship Network
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Disease: 1Symptom: 1Target: 6Links: 7
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 27817
- Core Entity Id
- 120385
- Source Entity Count
- 1
- Preferred Name
- Chromosomal Duplication
- Name Cn
- 染色体重复
- Name Pinyin
- Ran Se Ti Chong Fu
- Name En
- Chromosomal Duplication
- 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:An irregularity in the number of chromosomes, usually in the form of a gain of genetic material. (NCI)|MSH2017_2016_08_12:An aberration in which an extra chromosome or a chromosomal segment is made.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Chromosomal Duplication
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Me Sh
D058674
Umls
C1516516
Sym Map
SMDE07098
Itcmdb Generated
ITX-DISEASE-160B80ABBFF8
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Definition
NCI2016_02D:An irregularity in the number of chromosomes, usually in the form of a gain of genetic material. (NCI)|MSH2017_2016_08_12:An aberration in which an extra chromosome or a chromosomal segment is made.