DiseaseID 21784

先天性肌无力综合征4A型(慢通道型)

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
21784
Core Entity Id
80539
Source Entity Count
1
Preferred Name
Myasthenic Syndrome, Congenital, 4A, Slow-Channel
Name Cn
先天性肌无力综合征4A型(慢通道型)
Name Pinyin
Xian Tian Xing Ji Wu Li Zong He Zheng 4a Xing ( Man Tong Dao Xing )
Name En
Myasthenic Syndrome, Congenital, 4A, Slow-Channel
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, 4A, Slow-Channel
Role
preferred
Name
CMS Ia1, FORMERLY
Role
alias
Name
CMS1A1, FORMERLY
Role
alias
Name
CMS4A
Role
alias
Name
CONGENITAL MYASTHENIC SYNDROME TYPE Ia1, FORMERLY
Role
alias
Name
Congenital Myasthenic Syndrome 4A
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS025803
Umls
C4225413
Sym Map
SMDE01961
Do Class
DOID:630DOID:7
Dis Ge Net
C4225413
Umls Sty
T047
Tcmbank Disease
31369
Itcmdb Generated
ITX-DISEASE-6721A8FD5698

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