DiseaseID 7825

先天性高铁血红蛋白血症

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: 1Symptom: 11Target: 18Links: 35
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Record Fields

Scalar fields from the final disease record.

Disease Id
7825
Core Entity Id
64686
Source Entity Count
1
Preferred Name
Congenital Methemoglobinemia
Name Cn
先天性高铁血红蛋白血症
Name Pinyin
Xian Tian Xing Gao Tie Xue Hong Dan Bai Xue Zheng
Name En
Congenital Methemoglobinemia
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Hemic and Lymphatic Diseases
Do Class
Hpo Class
Mesh Class Name
Hemic and Lymphatic Diseases
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
Congenital Methemoglobinemia
Role
preferred
Name
Dihydrolipoamide Dehydrogenase Deficiency
Role
preferred
Name
Congenital Methaemoglobinaemia
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS006714
Umls
C0268193
Icd10
D74.0
Sym Map
SMDE00362
Dis Ge Net
C0272087
Umls Sty
T047
Me Sh Class
C15
Etcm Disease
Dihydrolipoamide Dehydrogenase Deficiency
Tcmbank Disease
23187
Itcmdb Generated
ITX-DISEASE-4002CBF53CBB

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Dihydrolipoamide Dehydrogenase Deficiency Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Dihydrolipoamide Dehydrogenase Deficiency
Global Category
Fetal diseases;Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Liver diseases;Nephrological diseases;Neuronal diseases
Me Sh Disease Class
Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or Syndrome