Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Target: 6Links: 6
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 15636
- Core Entity Id
- 73596
- Source Entity Count
- 1
- Preferred Name
- Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency
- Name Cn
- 致死性婴儿型心脑肌病，由细胞色素C氧化酶缺乏引起
- Name Pinyin
- Zhi Si Xing Ying Er Xing Xin Nao Ji Bing ， You Xi Bao Se Su C Yang Hua Mei Que Fa Yin Qi
- Name En
- Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
- Do Class
- genetic disease; disease of metabolism
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases
- Hpo Class Name
- Do Class Name
- disease of metabolism; genetic disease
- Disease Definition
- Version
- Suppressed
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency
Role
preferred
Name
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 1
Role
alias
Name
Cemcox1
Role
alias
Name
Fatal Infantile Cardioencephalomyopathy Due To Cytochrome C Oxidase Deficiency
Role
alias
Name
Fatal Infantile Cardioencephalomyopathy Due To Cytochrome C Oxidase Deficiency 1
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS017538
Omim
604377
Do Class
DOID:0014667DOID:630
Dis Ge Net
C1858424
Umls Sty
T047
Me Sh Class
C05C10C14C16C18
Tcmbank Disease
15748
Attributes
Merged source attributes and domain-specific metadata.
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
Me Sh Disease Class
Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases
Umls Semantic Type Name
Disease or Syndrome