DiseaseID 18662

常染色体显性遗传小脑性共济失调-耳聋-发作性睡病

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: 5Herb: 12Symptom: 5Target: 18Links: 46
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Record Fields

Scalar fields from the final disease record.

Disease Id
18662
Core Entity Id
77094
Source Entity Count
1
Preferred Name
Cerebellar Ataxia, Deafness, And Narcolepsy, Autosomal Dominant
Name Cn
常染色体显性遗传小脑性共济失调-耳聋-发作性睡病
Name Pinyin
Chang Ran Se Ti Xian Xing Yi Chuan Xiao Nao Xing Gong Ji Shi Tiao - Er Long - Fa Zuo Xing Shui Bing
Name En
Cerebellar Ataxia, Deafness, And Narcolepsy, Autosomal Dominant
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
Cerebellar Ataxia, Deafness, And Narcolepsy, Autosomal Dominant
Role
preferred
Name
ADCADN
Role
alias
Name
Autosomal Dominant Cerebellar Ataxia, Deafness And Narcolepsy
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS022252
Omim
604121
Umls
C3807295
Sym Map
SMDE02777
Do Class
DOID:630DOID:7
Dis Ge Net
C3807295
Umls Sty
T047
Etcm Disease
Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant
Tcmbank Disease
27007
Itcmdb Generated
ITX-DISEASE-02DDB823A68A

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant 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
Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Ear diseases;Neuronal diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome