DiseaseID 2556

肌营养不良-肌聚糖病(先天性伴脑眼异常),A型7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: 3Target: 1Links: 4
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Record Fields

Scalar fields from the final disease record.

Disease Id
2556
Core Entity Id
2893
Source Entity Count
1
Preferred Name
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 7
Name Cn
肌营养不良-肌聚糖病(先天性伴脑眼异常),A型7型
Name Pinyin
Ji Ying Yang Bu Liang - Ji Ju Tang Bing ( Xian Tian Xing Ban Nao Yan Yi Chang ),a Xing 7 Xing
Name En
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 7
Name Latin
Bilingual Status
complete
Disease Type
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
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, 7
Role
preferred
Name
Congenital Muscular Dystrophy-Dystroglycanopathy A7
Role
alias
Name
MDDGA7
Role
alias
Name
WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, ISPD-RELATED
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS029394
Omim
614643
Umls
C3553330
Sym Map
SMDE00096
Do Class
DOID:630DOID:7
Dis Ge Net
C3553330
Umls Sty
T047

Attributes

Merged source attributes and domain-specific metadata.

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