DiseaseID 18399

致死性婴儿心脏脑肌病2型,由细胞色素C氧化酶缺乏所致

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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: 1Herb: 1Target: 17Links: 25
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Record Fields

Scalar fields from the final disease record.

Disease Id
18399
Core Entity Id
76791
Source Entity Count
1
Preferred Name
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 2
Name Cn
致死性婴儿心脏脑肌病2型,由细胞色素C氧化酶缺乏所致
Name Pinyin
Zhi Si Xing Ying Er Xin Zang Nao Ji Bing 2 Xing , You Xi Bao Se Su C Yang Hua Mei Que Fa Suo Zhi
Name En
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 2
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Do Class
genetic disease; disease of metabolism
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
disease of metabolism; genetic disease
Disease Definition
Version
v1
Suppressed
No

Names

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

Name
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 2
Role
preferred
Name
CEMCOX2
Role
alias
Name
Fatal Infantile Cardioencephalomyopathy Due To Cytochrome C Oxidase Deficiency 2
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021867
Omim
615119
Umls
C3554534
Sym Map
SMDE01318
Do Class
DOID:0014667DOID:630
Dis Ge Net
C3554534
Umls Sty
T047
Etcm Disease
Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2
Tcmbank Disease
2687
Itcmdb Generated
ITX-DISEASE-16127D5EEFD2

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2 Details page
Do Class Name
disease of metabolism; genetic disease
Disease Type
disease
Do Disease Class
genetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2
Global Category
Genetic diseases;Metabolic diseases
Anatomical Category
Cardiovascular diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome