DiseaseID 25842
致死性婴儿心脏脑肌病，由细胞色素C氧化酶缺乏1型引起
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 1
Relationship Network
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Disease: 1Formula: 5Symptom: 1Target: 16Links: 30
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 25842
- Core Entity Id
- 118410
- Source Entity Count
- 1
- Preferred Name
- Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 1
- Name Cn
- 致死性婴儿心脏脑肌病，由细胞色素C氧化酶缺乏1型引起
- Name Pinyin
- Zhi Si Xing Ying Er Xin Zang Nao Ji Bing ， You Xi Bao Se Su C Yang Hua Mei Que Fa 1 Xing Yin Qi
- Name En
- Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 1
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- 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 1
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C1858424
Sym Map
SMDE00575
Etcm Disease
Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1
Itcmdb Generated
ITX-DISEASE-6DF89EDB0D3A
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 Details page
Basic Information
Disease Name
Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1
Global Category
Genetic diseases;Metabolic diseases
Anatomical Category
Cardiovascular diseases;Neuronal diseases