DiseaseID 25970
肢带型肌营养不良2D型
Muscular Dystrophy, Limb-Girdle, Type 2D
MSH2017_2016_08_12:Limb girdle muscular dystrophies due to mutations in the gene for the ALPHA-SARCOGLYCAN or deficiencies in alpha-sarcoglycan due to a mutation in another gene (secondary alpha-sarcoglycanopathy).
Relationship Network
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Disease: 1Symptom: 1Target: 8Links: 9
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 25970
- Core Entity Id
- 118538
- Source Entity Count
- 1
- Preferred Name
- Muscular Dystrophy, Limb-Girdle, Type 2D
- Name Cn
- 肢带型肌营养不良2D型
- Name Pinyin
- Zhi Dai Xing Ji Ying Yang Bu Liang 2d Xing
- Name En
- Muscular Dystrophy, Limb-Girdle, Type 2D
- 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:Limb girdle muscular dystrophies due to mutations in the gene for the ALPHA-SARCOGLYCAN or deficiencies in alpha-sarcoglycan due to a mutation in another gene (secondary alpha-sarcoglycanopathy).
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Muscular Dystrophy, Limb-Girdle, Type 2D
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Umls
C2936332
Sym Map
SMDE01333
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Definition
MSH2017_2016_08_12:Limb girdle muscular dystrophies due to mutations in the gene for the ALPHA-SARCOGLYCAN or deficiencies in alpha-sarcoglycan due to a mutation in another gene (secondary alpha-sarcoglycanopathy).