DiseaseID 26627

10型Leber先天性黑矇

Leber Congenital Amaurosis 10

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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: 4Target: 18Links: 28
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
26627
Core Entity Id
119195
Source Entity Count
1
Preferred Name
Leber Congenital Amaurosis 10
Name Cn
10型Leber先天性黑矇
Name Pinyin
10 Xing Leber Xian Tian Xing Hei Meng
Name En
Leber Congenital Amaurosis 10
Name Latin
Bilingual Status
complete
Disease Type
Umls Disease Type
Disgenet Type
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
Leber Congenital Amaurosis 10
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Umls
C1857821
Sym Map
SMDE04419
Etcm Disease
Leber Congenital Amaurosis 10
Itcmdb Generated
ITX-DISEASE-5F20975C39D3

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Leber Congenital Amaurosis 10 Details page
Basic Information
Disease Name
Leber Congenital Amaurosis 10
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases;Neuronal diseases