DiseaseID 18715

家族性成人肌阵挛性癫痫5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: 5Target: 19Links: 29
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Record Fields

Scalar fields from the final disease record.

Disease Id
18715
Core Entity Id
77156
Source Entity Count
1
Preferred Name
Epilepsy, Familial Adult Myoclonic, 5
Name Cn
家族性成人肌阵挛性癫痫5型
Name Pinyin
Jia Zu Xing Cheng Ren Ji Zhen Luan Xing Dian Xian 5 Xing
Name En
Epilepsy, Familial Adult Myoclonic, 5
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Do Class
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
Version
v1,v2
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Epilepsy, Familial Adult Myoclonic, 5
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS022341
Omim
615400
Umls
C3809374
Sym Map
SMDE02944
Dis Ge Net
C3809374
Umls Sty
T047
Etcm Disease
Epilepsy, Familial Adult Myoclonic, 5
Tcmbank Disease
19101
Itcmdb Generated
ITX-DISEASE-CCA0A53A4225

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Epilepsy, Familial Adult Myoclonic, 5 Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Epilepsy, Familial Adult Myoclonic, 5
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Neuronal diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome