DiseaseID 18685

先天性肌无力综合征8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
18685
Core Entity Id
77120
Source Entity Count
1
Preferred Name
Myasthenic Syndrome, Congenital, 8
Name Cn
先天性肌无力综合征8型
Name Pinyin
Xian Tian Xing Ji Wu Li Zong He Zheng 8 Xing
Name En
Myasthenic Syndrome, Congenital, 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
Myasthenic Syndrome, Congenital, 8
Role
preferred
Name
CMS8
Role
alias
Name
CMSPPD
Role
alias
Name
Congenital Myasthenic Syndrome 8
Role
alias
Name
MYASTHENIC SYNDROME, CONGENITAL, DUE TO AGRIN DEFICIENCY
Role
alias
Name
MYASTHENIC SYNDROME, CONGENITAL, WITH PRE- AND POSTSYNAPTIC DEFECTS
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS022286
Omim
615120
Umls
C3808739
Sym Map
SMDE00038
Do Class
DOID:630DOID:7
Dis Ge Net
C3808739
Umls Sty
T047
Tcmbank Disease
6767

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