DiseaseID 21718

肌肉萎缩症-抗肌萎缩相关糖蛋白病(先天性伴脑和眼异常),A型,9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: 2Target: 1Links: 3
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Record Fields

Scalar fields from the final disease record.

Disease Id
21718
Core Entity Id
80462
Source Entity Count
1
Preferred Name
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 9
Name Cn
肌肉萎缩症-抗肌萎缩相关糖蛋白病(先天性伴脑和眼异常),A型,9型
Name Pinyin
Ji Rou Wei Suo Zheng - Kang Ji Wei Suo Xiang Guan Tang Dan Bai Bing ( Xian Tian Xing Ban Nao He Yan Yi Chang ),a Xing ,9 Xing
Name En
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 9
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
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, 9
Role
preferred
Name
Congenital Muscular Dystrophy-Dystroglycanopathy Type A9
Role
alias
Name
MDDGA9
Role
alias
Name
WALKER-WARBURG SYNDROME OR MUSCLE-EYE BRAIN DISEASE, DAG1-RELATED
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS025705
Omim
616538
Umls
C4225291
Sym Map
SMDE00991
Do Class
DOID:630DOID:7
Dis Ge Net
C4225291
Umls Sty
T047
Tcmbank Disease
2967

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
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