DiseaseID 17722

先天性红细胞生成异常性贫血IV型

disease

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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
17722
Core Entity Id
76002
Source Entity Count
1
Preferred Name
Congenital Dyserythropoietic Anemia Type Iv
Name Cn
先天性红细胞生成异常性贫血IV型
Name Pinyin
Xian Tian Xing Hong Xi Bao Sheng Cheng Yi Chang Xing Pin Xue Iv Xing
Name En
Congenital Dyserythropoietic Anemia Type Iv
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Do Class
disease of anatomical entity; genetic disease
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Hpo Class Name
Do Class Name
genetic disease; disease of anatomical entity
Disease Definition
Version
Suppressed

Names

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

Name
Congenital Dyserythropoietic Anemia Type Iv
Role
preferred
Name
Anemia, Congenital Dyserythropoietic, Type Iv
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS020714
Omim
613673
Do Class
DOID:630DOID:7
Dis Ge Net
C3150926
Umls Sty
T047
Me Sh Class
C15C16
Tcmbank Disease
29428

Attributes

Merged source attributes and domain-specific metadata.

Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or Syndrome