DiseaseID 21684

视神经萎缩10型伴或不伴共济失调、精神发育迟滞和癫痫发作

disease

Back to Browse

Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

Click a node to open it in a new tab
Disease: 1Symptom: 2Target: 1Links: 3
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
21684
Core Entity Id
80425
Source Entity Count
1
Preferred Name
Optic Atrophy 10 With Or Without Ataxia, Mental Retardation, And Seizures
Name Cn
视神经萎缩10型伴或不伴共济失调、精神发育迟滞和癫痫发作
Name Pinyin
Shi Shen Jing Wei Suo 10 Xing Ban Huo Bu Ban Gong Ji Shi Tiao 、 Jing Shen Fa Yu Chi Zhi He Dian Xian Fa Zuo
Name En
Optic Atrophy 10 With Or Without Ataxia, Mental Retardation, And Seizures
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
Optic Atrophy 10 With Or Without Ataxia, Mental Retardation, And Seizures
Role
preferred
Name
OPA10
Role
alias
Name
Optic Atrophy 10
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS025657
Omim
616732
Umls
C4225227
Sym Map
SMDE00025
Do Class
DOID:630DOID:7
Dis Ge Net
C4225227
Umls Sty
T047
Tcmbank Disease
8272

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