Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 1Target: 12Links: 13
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 6329
- Core Entity Id
- 62963
- Source Entity Count
- 1
- Preferred Name
- Xanthinuria
- Name Cn
- 黄嘌呤尿症
- Name Pinyin
- Huang Piao Ling Niao Zheng
- Name En
- Xanthinuria
- 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
- genetic disease; disease of metabolism
- Hpo Class
- Abnormality of metabolism/homeostasisAbnormality of metabolism/homeostasis; Abnormality of the genitourinary system
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
- Hpo Class Name
- Abnormality of metabolism/homeostasisAbnormality of metabolism/homeostasis; Abnormality of the genitourinary system
- Do Class Name
- disease of metabolism; genetic disease
- Disease Definition
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Xanthinuria
Role
preferred
Name
Xanthinuria, Type I
Role
preferred
Name
Reduced Xanthine Dehydrogenase Activity
Role
preferred
Name
Xanthinuria, Type II
Role
preferred
Name
Increased Urinary Xanthine
Role
alias
Name
Purine-Pyrimidine Metabolic Disorder
Role
alias
Name
XAN1
Role
alias
Name
XANTHINE DEHYDROGENASE DEFICIENCY
Role
alias
Name
XANTHINE OXIDASE DEFICIENCY
Role
alias
Name
XDH DEFICIENCY
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0003534HP:0010934
Herb
HBDIS004539HBDIS006180HBDIS018047HBDIS025054
Omim
278300603592
Umls
C0268118
Sym Map
SMDE04549
Do Class
DOID:0014667DOID:630
Dis Ge Net
C0220988C0268118C1863688C4025600
Umls Sty
T033T047
Hpo Class
HP:0000119HP:0001939
Me Sh Class
C16C18
Tcmbank Disease
1082112006156111962323726529
Itcmdb Generated
ITX-DISEASE-20C626AE1DEAITX-DISEASE-533332BD64C8
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Do Class Name
disease of metabolism; genetic disease
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of metabolism/homeostasisAbnormality of metabolism/homeostasis; Abnormality of the genitourinary system
Do Disease Class
genetic disease; disease of metabolism
Hpo Disease Class
Abnormality of metabolism/homeostasisAbnormality of metabolism/homeostasis; Abnormality of the genitourinary system
Umls Disease Type
Disease or SyndromeFinding
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or SyndromeFinding