DiseaseID 21759

先天性肌无力综合征3C型伴乙酰胆碱受体缺陷

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
21759
Core Entity Id
80511
Source Entity Count
1
Preferred Name
Myasthenic Syndrome, Congenital, 3C, Associated With Acetylcholine Receptor Deficiency
Name Cn
先天性肌无力综合征3C型伴乙酰胆碱受体缺陷
Name Pinyin
Xian Tian Xing Ji Wu Li Zong He Zheng 3c Xing Ban Yi Xian Dan Jian Shou Ti Que Xian
Name En
Myasthenic Syndrome, Congenital, 3C, Associated With Acetylcholine Receptor Deficiency
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, 3C, Associated With Acetylcholine Receptor Deficiency
Role
preferred
Name
CMS3C
Role
alias
Name
Congenital Myasthenic Syndrome 3C
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS025770
Omim
616323
Umls
C4225370
Sym Map
SMDE03801
Do Class
DOID:630DOID:7
Dis Ge Net
C4225370
Umls Sty
T047
Tcmbank Disease
26317

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