DiseaseID 26389

先天性Rett综合征变异型

Rett Syndrome, Congenital Variant

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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: 9Target: 1Links: 10
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Record Fields

Scalar fields from the final disease record.

Disease Id
26389
Core Entity Id
118957
Source Entity Count
1
Preferred Name
Rett Syndrome, Congenital Variant
Name Cn
先天性Rett综合征变异型
Name Pinyin
Xian Tian Xing Rett Zong He Zheng Bian Yi Xing
Name En
Rett Syndrome, Congenital Variant
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
Rett Syndrome, Congenital Variant
Role
preferred
Source
SymMap_v2
Preferred
Yes

Cross References

Trusted external identifiers retained for this final record.

Umls
C3150705
Sym Map
SMDE03251

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0