DiseaseID 26590

莱伯先天性黑矇1型

Leber Congenital Amaurosis 1

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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: 8Target: 20Links: 32
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
26590
Core Entity Id
119158
Source Entity Count
1
Preferred Name
Leber Congenital Amaurosis 1
Name Cn
莱伯先天性黑矇1型
Name Pinyin
Lai Bo Xian Tian Xing Hei Meng 1 Xing
Name En
Leber Congenital Amaurosis 1
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 1
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Umls
C2931258
Sym Map
SMDE04208
Etcm Disease
Leber Congenital Amaurosis 1
Itcmdb Generated
ITX-DISEASE-1E9E4D7EABAC

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Leber Congenital Amaurosis 1 Details page
Basic Information
Disease Name
Leber Congenital Amaurosis 1
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases;Neuronal diseases