DiseaseID 7530

果糖激酶缺乏症

disease

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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
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Record Fields

Scalar fields from the final disease record.

Disease Id
7530
Core Entity Id
64334
Source Entity Count
1
Preferred Name
Deficiency of Fructokinase
Name Cn
果糖激酶缺乏症
Name Pinyin
Guo Tang Ji Mei Que Fa Zheng
Name En
Deficiency of Fructokinase
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
Suppressed

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Deficiency of Fructokinase
Role
preferred
Name
Essential Benign Fructosuria
Role
alias
Name
Fructosuria
Role
alias
Name
Fructosuria, Essential
Role
alias
Name
Hepatic Fructokinase Deficiency
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS006203
Omim
229800
Dis Ge Net
C0268160
Umls Sty
T047
Me Sh Class
C16C18
Tcmbank Disease
7592

Attributes

Merged source attributes and domain-specific metadata.

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