Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 6Symptom: 6Target: 18Links: 36
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 8893
- Core Entity Id
- 65889
- Source Entity Count
- 1
- Preferred Name
- Dihydropyrimidinuria
- Name Cn
- 二氢嘧啶尿症
- Name Pinyin
- Er Qing Mi Ding Niao Zheng
- Name En
- Dihydropyrimidinuria
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Chemically-Induced DisordersCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
- Do Class
- genetic disease; disease of metabolism
- Hpo Class
- Abnormality of metabolism/homeostasis
- Mesh Class Name
- Chemically-Induced DisordersCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
- Hpo Class Name
- Abnormality of metabolism/homeostasis
- Do Class Name
- disease of metabolism; genetic disease
- Disease Definition
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Dihydropyrimidinuria
Role
preferred
Name
Dihydropyrimidinase Deficiency
Role
preferred
Name
Dihydropyrimidine Dehydrogenase Deficiency
Role
preferred
Name
Poisoning By Fluorouracil
Role
preferred
Name
Reduced Dihydropyrimidine Dehydrogenase Activity
Role
preferred
Name
5-FLUOROURACIL TOXICITY
Role
alias
Name
DPD DEFICIENCY
Role
alias
Name
DPH DEFICIENCY
Role
alias
Name
DPYD DEFICIENCY
Role
alias
Name
DPYS DEFICIENCY
Role
alias
Name
DPYSD
Role
alias
Name
PYRIMIDINEMIA, FAMILIAL
Role
alias
Name
THYMINE-URACILURIA, HEREDITARY
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0003654
Herb
HBDIS006788HBDIS008082HBDIS018597HBDIS021508HBDIS025040
Me Sh
D054067
Omim
222748274270
Umls
C0274576C0342803C1959620C3495551
Sym Map
SMDE03094SMDE04181SMDE07920
Do Class
DOID:0014667DOID:630
Dis Ge Net
C0274576C0342803C1959620C3495551C4025582
Umls Sty
T033T037T047
Hpo Class
HP:0001939
Me Sh Class
C16C18C25
Etcm Disease
Dihydropyrimidinase DeficiencyDihydropyrimidine Dehydrogenase Deficiency
Tcmbank Disease
12610250023239949826179
Itcmdb Generated
ITX-DISEASE-161FD966A60BITX-DISEASE-4ED56841A0F5ITX-DISEASE-A00B135CE453
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2v2
Suppress
0
Page Title
Disease Dihydropyrimidinase Deficiency Details pageDisease Dihydropyrimidine Dehydrogenase Deficiency Details page
Do Class Name
disease of metabolism; genetic disease
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of metabolism/homeostasis
Do Disease Class
genetic disease; disease of metabolism
Hpo Disease Class
Abnormality of metabolism/homeostasis
Umls Disease Type
Disease or SyndromeFindingInjury or Poisoning
Basic Information
Disease Name
Dihydropyrimidinase Deficiency
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Gastrointestinal Diseases;Neuronal diseases
Disease Name
Dihydropyrimidine Dehydrogenase Deficiency
Global Category
Cancer diseases;Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Blood diseases;Bone diseases;Mental diseases;Neuronal diseases
Me Sh Disease Class
Chemically-Induced DisordersCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Chemically-Induced DisordersCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or SyndromeFindingInjury or Poisoning