DiseaseID 25732
变异型Aβ2M淀粉样变性
Variant Abeta2M Amyloidosis
#946;2M) leading to progressive gastrointestinal dysfunction, Sj？gren syndrome (see this term) and autonomic neuropathy.
Relationship Network
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Disease: 1Symptom: 7Target: 1Links: 8
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 25732
- Core Entity Id
- 118300
- Source Entity Count
- 1
- Preferred Name
- Variant Abeta2M Amyloidosis
- Name Cn
- 变异型Aβ2M淀粉样变性
- Name Pinyin
- Bian Yi Xing Aβ2m Dian Fen Yang Bian Xing
- Name En
- Variant Abeta2M Amyloidosis
- 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
- #946;2M) leading to progressive gastrointestinal dysfunction, Sj？gren syndrome (see this term) and autonomic neuropathy.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Variant Abeta2M Amyloidosis
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Sym Map
SMDE00106
Orphanet
314652
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Definition
#946;2M) leading to progressive gastrointestinal dysfunction, Sj？gren syndrome (see this term) and autonomic neuropathy.