Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 9Target: 5Links: 14
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 16542
- Core Entity Id
- 74635
- Source Entity Count
- 1
- Preferred Name
- Phosphoglycerate Kinase 1 Deficiency
- Name Cn
- 磷酸甘油酸激酶1缺乏症
- Name Pinyin
- Lin Suan Gan You Suan Ji Mei 1 Que Fa Zheng
- Name En
- Phosphoglycerate Kinase 1 Deficiency
- 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,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Phosphoglycerate Kinase 1 Deficiency
Role
preferred
Name
PGK1 DEFICIENCY
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS018865
Omim
300653
Umls
C1970848
Sym Map
SMDE03911
Dis Ge Net
C1970848
Umls Sty
T047
Me Sh Class
C16C18
Tcmbank Disease
15407
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
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