DiseaseID 26455

严重先天性中性粒细胞减少症2型,常染色体显性遗传

Neutropenia, Severe Congenital, 2, 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: 1Target: 2Links: 2
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Record Fields

Scalar fields from the final disease record.

Disease Id
26455
Core Entity Id
119023
Source Entity Count
1
Preferred Name
Neutropenia, Severe Congenital, 2, Autosomal Dominant
Name Cn
严重先天性中性粒细胞减少症2型,常染色体显性遗传
Name Pinyin
Yan Zhong Xian Tian Xing Zhong Xing Li Xi Bao Jian Shao Zheng 2 Xing , Chang Ran Se Ti Xian Xing Yi Chuan
Name En
Neutropenia, Severe Congenital, 2, 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
Neutropenia, Severe Congenital, 2, Autosomal Dominant
Role
preferred
Source
SymMap_v2
Preferred
Yes

Cross References

Trusted external identifiers retained for this final record.

Umls
C2751288
Sym Map
SMDE03566

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0