Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Target: 1Links: 1
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 2518
- Core Entity Id
- 2846
- Source Entity Count
- 1
- Preferred Name
- Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency
- Name Cn
- 新生儿线粒体脑心肌病(ATP合酶缺乏所致)
- Name Pinyin
- Xin Sheng Er Xian Li Ti Nao Xin Ji Bing (atp He Mei Que Fa Suo Zhi )
- Name En
- Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Nervous System Diseases; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
- Do Class
- genetic disease; disease of metabolism
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- Version
- Suppressed
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency
Role
preferred
Name
Mitochondrial Complex V (Atp Synthase) Deficiency Nuclear Type 2
Role
alias
Name
Mitochondrial Complex V (Atp Synthase) Deficiency, Nuclear Type 2
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS029322
Omim
614052
Do Class
DOID:0014667DOID:630
Dis Ge Net
C3279699
Umls Sty
T047
Me Sh Class
C05C10C18
Attributes
Merged source attributes and domain-specific metadata.
Do Disease Class
genetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Nervous System Diseases; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Dis Ge Net Disease Type
disease