DiseaseID 33183

常染色体显性遗传近视20型

Myopia 20, Autosomal Dominant

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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: 1Herb: 7Target: 16Links: 31
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Record Fields

Scalar fields from the final disease record.

Disease Id
33183
Core Entity Id
193117
Source Entity Count
1
Preferred Name
Myopia 20, Autosomal Dominant
Name Cn
常染色体显性遗传近视20型
Name Pinyin
Chang Ran Se Ti Xian Xing Yi Chuan Jin Shi 20 Xing
Name En
Myopia 20, Autosomal Dominant
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
Suppressed

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Myopia 20, Autosomal Dominant
Role
preferred
Source
ETCM_v2
Preferred
Yes

Cross References

Trusted external identifiers retained for this final record.

Etcm Disease
Myopia 20, Autosomal Dominant
Itcmdb Generated
ITX-DISEASE-BB5813C1E646

Attributes

Merged source attributes and domain-specific metadata.

Page Title
Disease Myopia 20, Autosomal Dominant Details page
Basic Information
Disease Name
Myopia 20, Autosomal Dominant
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases