DiseaseID 17671

肌营养不良-肌营养不良蛋白聚糖病(先天性伴脑眼异常)A型5型

disease

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Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

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Disease: 1Symptom: 1Target: 1Links: 2
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Record Fields

Scalar fields from the final disease record.

Disease Id
17671
Core Entity Id
75944
Source Entity Count
1
Preferred Name
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 5
Name Cn
肌营养不良-肌营养不良蛋白聚糖病(先天性伴脑眼异常)A型5型
Name Pinyin
Ji Ying Yang Bu Liang - Ji Ying Yang Bu Liang Dan Bai Ju Tang Bing ( Xian Tian Xing Ban Nao Yan Yi Chang )a Xing 5 Xing
Name En
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 5
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Do Class
disease of anatomical entity; genetic disease
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
genetic disease; disease of anatomical entity
Disease Definition
Version
v1,v2
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 5
Role
preferred
Name
Congenital Muscular Dystrophy-Dystroglycanopathy Type A5
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS020631
Omim
613153
Umls
C3150413
Sym Map
SMDE03146
Do Class
DOID:630DOID:7
Dis Ge Net
C3150413
Umls Sty
T047
Tcmbank Disease
1987

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome