DiseaseID 15541

2,4-二烯酰辅酶A还原酶缺乏症

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: 1Formula: 18Symptom: 4Target: 36Links: 58
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Record Fields

Scalar fields from the final disease record.

Disease Id
15541
Core Entity Id
73489
Source Entity Count
1
Preferred Name
2,4-Dienoyl-Coa Reductase Deficiency
Name Cn
2,4-二烯酰辅酶A还原酶缺乏症
Name Pinyin
2,4- Er Xi Xian Fu Mei A Huan Yuan Mei Que Fa Zheng
Name En
2,4-Dienoyl-Coa Reductase Deficiency
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; Nutritional and Metabolic Diseases
Do Class
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic 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
2,4-Dienoyl-Coa Reductase Deficiency
Role
preferred
Name
DECRD
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS017397
Omim
616034
Umls
C1857252
Sym Map
SMDE00803
Dis Ge Net
C1857252
Umls Sty
T047
Me Sh Class
C16C18
Etcm Disease
2,4-Dienoyl-Coa Reductase Deficiency
Tcmbank Disease
11646
Itcmdb Generated
ITX-DISEASE-9A58BBCD04FE

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease 2,4-Dienoyl-Coa Reductase Deficiency Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
2,4-Dienoyl-Coa Reductase Deficiency
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Neuronal diseases
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or Syndrome