DiseaseID 21754

先天性肌无力综合征18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
21754
Core Entity Id
80505
Source Entity Count
1
Preferred Name
Myasthenic Syndrome, Congenital, 18
Name Cn
先天性肌无力综合征18型
Name Pinyin
Xian Tian Xing Ji Wu Li Zong He Zheng 18 Xing
Name En
Myasthenic Syndrome, Congenital, 18
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
Myasthenic Syndrome, Congenital, 18
Role
preferred
Name
CMS18
Role
alias
Name
Congenital Myasthenic Syndrome 18
Role
alias
Name
MYASTHENIC SYNDROME, CONGENITAL, 18, WITH INTELLECTUAL DISABILITY AND ATAXIA
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS025765
Omim
616330
Umls
C4225364
Sym Map
SMDE01298
Do Class
DOID:630DOID:7
Dis Ge Net
C4225364
Umls Sty
T047
Tcmbank Disease
3663

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