DiseaseID 18704

肌营养不良-抗肌萎缩相关糖蛋白病(先天伴脑眼异常)A14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: 4Target: 1Links: 5
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Record Fields

Scalar fields from the final disease record.

Disease Id
18704
Core Entity Id
77143
Source Entity Count
1
Preferred Name
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 14
Name Cn
肌营养不良-抗肌萎缩相关糖蛋白病(先天伴脑眼异常)A14型
Name Pinyin
Ji Ying Yang Bu Liang - Kang Ji Wei Suo Xiang Guan Tang Dan Bai Bing ( Xian Tian Ban Nao Yan Yi Chang )a14 Xing
Name En
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 14
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, 14
Role
preferred
Name
Congenital Muscular Dystrophy-Dystroglycanopathy A14
Role
alias
Name
MDDGA14
Role
alias
Name
WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, GMPPB-RELATED
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS022326
Omim
615350
Umls
C3809216
Sym Map
SMDE03181
Do Class
DOID:630DOID:7
Dis Ge Net
C3809216
Umls Sty
T047
Tcmbank Disease
5872

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