DiseaseID 25953

常染色体显性遗传性Klippel-Feil综合征1型

Klippel-Feil Syndrome 1, Autosomal Dominant

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Relationship Network

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Disease: 1Target: 7Links: 7
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Record Fields

Scalar fields from the final disease record.

Disease Id
25953
Core Entity Id
118521
Source Entity Count
1
Preferred Name
Klippel-Feil Syndrome 1, Autosomal Dominant
Name Cn
常染色体显性遗传性Klippel-Feil综合征1型
Name Pinyin
Chang Ran Se Ti Xian Xing Yi Chuan Xing Klippel-feil Zong He Zheng 1 Xing
Name En
Klippel-Feil Syndrome 1, 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
v1
Suppressed
No

Names

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

Name
Klippel-Feil Syndrome 1, Autosomal Dominant
Role
preferred
Source
SymMap_v2
Preferred
Yes

Cross References

Trusted external identifiers retained for this final record.

Umls
C1861689
Sym Map
SMDE01241

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0