DiseaseID 31527

20p13微缺失综合征

20p13 Microdeletion Syndrome

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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: 1Target: 35Links: 35
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Record Fields

Scalar fields from the final disease record.

Disease Id
31527
Core Entity Id
191461
Source Entity Count
1
Preferred Name
20p13 Microdeletion Syndrome
Name Cn
20p13微缺失综合征
Name Pinyin
20p13 Wei Que Shi Zong He Zheng
Name En
20p13 Microdeletion Syndrome
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
20p13 Microdeletion Syndrome
Role
preferred
Source
ETCM_v2
Preferred
Yes

Cross References

Trusted external identifiers retained for this final record.

Etcm Disease
20p13 Microdeletion Syndrome
Itcmdb Generated
ITX-DISEASE-AFBD8BF1DBA3

Attributes

Merged source attributes and domain-specific metadata.

Page Title
Disease 20p13 Microdeletion Syndrome Details page
Basic Information
Disease Name
20p13 Microdeletion Syndrome
Global Category
Fetal diseases;Rare diseases
Anatomical Category
Neuronal diseases