DiseaseID 926

家族性颞叶癫痫1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: 1Formula: 17Herb: 12Target: 19Links: 53
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Record Fields

Scalar fields from the final disease record.

Disease Id
926
Core Entity Id
1047
Source Entity Count
1
Preferred Name
Epilepsy, Familial Temporal Lobe 1
Name Cn
家族性颞叶癫痫1型
Name Pinyin
Jia Zu Xing Nie Ye Dian Xian 1 Xing
Name En
Epilepsy, Familial Temporal Lobe 1
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Do Class
disease of anatomical entity; genetic disease
Hpo Class
Mesh Class Name
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders
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
Epilepsy, Familial Temporal Lobe 1
Role
preferred
Name
Epilepsy, Familial Temporal Lobe, 1
Role
preferred
Name
Epilepsy, Familial Temporal Lobe, 8
Role
preferred
Name
Autosomal Dominant Lateral Temporal Lobe Epilepsy
Role
preferred
Name
EPILEPSY, FAMILIAL TEMPORAL LOBE, 7
Role
preferred
Name
ADLTE
Role
alias
Name
ADPEAF
Role
alias
Name
EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT
Role
alias
Name
EPILEPSY, PARTIAL, WITH AUDITORY FEATURES
Role
alias
Name
ETL1
Role
alias
Name
ETL8
Role
alias
Name
Familial Temporal Lobe Epilepsy 1
Role
alias
Name
Familial Temporal Lobe Epilepsy 7
Role
alias
Name
Familial Temporal Lobe Epilepsy 8
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS015644HBDIS025726HBDIS025733HBDIS027351
Omim
600512616436616461
Umls
C1838062C4225318
Sym Map
SMDE03788SMDE04385
Do Class
DOID:630DOID:7
Dis Ge Net
C1838062C4225318C4225327C4551957
Umls Sty
T047
Me Sh Class
C10C23F03
Etcm Disease
Epilepsy, Familial Temporal Lobe, 1Epilepsy, Familial Temporal Lobe, 7Epilepsy, Familial Temporal Lobe, 8
Tcmbank Disease
16446276013008930816
Itcmdb Generated
ITX-DISEASE-040329EBED2DITX-DISEASE-0E18F1F1F2D8ITX-DISEASE-E0B48DE85B3F

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Epilepsy, Familial Temporal Lobe, 1 Details pageDisease Epilepsy, Familial Temporal Lobe, 7 Details pageDisease Epilepsy, Familial Temporal Lobe, 8 Details page
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
Basic Information
Disease Name
Epilepsy, Familial Temporal Lobe, 1
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Neuronal diseases
Disease Name
Epilepsy, Familial Temporal Lobe, 7
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Neuronal diseases
Disease Name
Epilepsy, Familial Temporal Lobe, 8
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Neuronal diseases
Me Sh Disease Class
Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders
Umls Semantic Type Name
Disease or Syndrome