DiseaseID 29740
金属代谢先天性缺陷
Metal Metabolism, Inborn Errors
MSH2017_2016_08_12:Dysfunctions in the metabolism of metals resulting from inborn genetic mutations that are inherited or acquired in utero.|CSP2006:genetically determined biochemical disorders in metal absorption, metal
Relationship Network
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Disease: 1Symptom: 2Target: 12Links: 14
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 29740
- Core Entity Id
- 122308
- Source Entity Count
- 1
- Preferred Name
- Metal Metabolism, Inborn Errors
- Name Cn
- 金属代谢先天性缺陷
- Name Pinyin
- Jin Shu Dai Xie Xian Tian Xing Que Xian
- Name En
- Metal Metabolism, Inborn Errors
- 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
- MSH2017_2016_08_12:Dysfunctions in the metabolism of metals resulting from inborn genetic mutations that are inherited or acquired in utero.|CSP2006:genetically determined biochemical disorders in metal absorption, metal excretion, metal transport, or incorporation of metal to protein or enzyme.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Metal Metabolism, Inborn Errors
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Me Sh
D008664
Umls
C0025534
Sym Map
SMDE10941
Itcmdb Generated
ITX-DISEASE-D5707C602488
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Definition
MSH2017_2016_08_12:Dysfunctions in the metabolism of metals resulting from inborn genetic mutations that are inherited or acquired in utero.|CSP2006:genetically determined biochemical disorders in metal absorption, metal excretion, metal transport, or incorporation of metal to protein or enzyme.