DiseaseID 18698

严重先天性中性粒细胞减少症5型,常染色体隐性

disease

Back to Browse

Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

Click a node to open it in a new tab
Disease: 1Symptom: 4Target: 2Links: 6
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
18698
Core Entity Id
77136
Source Entity Count
1
Preferred Name
Neutropenia, Severe Congenital, 5, Autosomal Recessive
Name Cn
严重先天性中性粒细胞减少症5型,常染色体隐性
Name Pinyin
Yan Zhong Xian Tian Xing Zhong Xing Li Xi Bao Jian Shao Zheng 5 Xing , Chang Ran Se Ti Yin Xing
Name En
Neutropenia, Severe Congenital, 5, Autosomal Recessive
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
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
Neutropenia, Severe Congenital, 5, Autosomal Recessive
Role
preferred
Name
SCN5
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS022314
Omim
615285
Umls
C3809031
Sym Map
SMDE04984
Dis Ge Net
C3809031
Umls Sty
T047
Tcmbank Disease
14547

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome