DiseaseID 18356

肌营养不良-肌聚糖病(先天性伴脑眼异常)A型8

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: 1Target: 2Links: 2
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Record Fields

Scalar fields from the final disease record.

Disease Id
18356
Core Entity Id
76743
Source Entity Count
1
Preferred Name
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 8
Name Cn
肌营养不良-肌聚糖病(先天性伴脑眼异常)A型8
Name Pinyin
Ji Ying Yang Bu Liang - Ji Ju Tang Bing ( Xian Tian Xing Ban Nao Yan Yi Chang )a Xing 8
Name En
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 8
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, 8
Role
preferred
Name
Congenital Muscular Dystrophy-Dystroglycanopathy Type A8
Role
alias
Name
MDDGA8
Role
alias
Name
WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, GTDC2-RELATED
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021787
Omim
614830
Umls
C3553813
Sym Map
SMDE01994
Do Class
DOID:630DOID:7
Dis Ge Net
C3553813
Umls Sty
T047
Tcmbank Disease
26739

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