DiseaseID 26557

先天性去糖基化障碍

Congenital Disorder Of Deglycosylation

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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: 12Target: 18Links: 36
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Record Fields

Scalar fields from the final disease record.

Disease Id
26557
Core Entity Id
119125
Source Entity Count
1
Preferred Name
Congenital Disorder Of Deglycosylation
Name Cn
先天性去糖基化障碍
Name Pinyin
Xian Tian Xing Qu Tang Ji Hua Zhang Ai
Name En
Congenital Disorder Of Deglycosylation
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
Congenital Disorder Of Deglycosylation
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Umls
C3808991
Sym Map
SMDE04044
Etcm Disease
Congenital Disorder of Deglycosylation
Itcmdb Generated
ITX-DISEASE-537C4E70D301

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Congenital Disorder of Deglycosylation Details page
Basic Information
Disease Name
Congenital Disorder of Deglycosylation
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Eye diseases;Liver diseases;Neuronal diseases;Skin diseases