Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Target: 2Links: 2
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 14985
- Core Entity Id
- 72854
- Source Entity Count
- 1
- Preferred Name
- Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial
- Name Cn
- 线粒体磷酸烯醇丙酮酸羧激酶缺乏症
- Name Pinyin
- Xian Li Ti Lin Suan Xi Chun Bing Tong Suan Suo Ji Mei Que Fa Zheng
- Name En
- Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial
- 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
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial
Role
preferred
Name
PCK2 DEFICIENCY
Role
alias
Name
PEPCK2 DEFICIENCY
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS016654
Omim
261650
Umls
C1849821
Sym Map
SMDE02772
Dis Ge Net
C1849821
Umls Sty
T047
Me Sh Class
C16C18
Tcmbank Disease
24738
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
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