DiseaseID 7591

羟犬尿氨酸尿症

phenotype

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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: 1Symptom: 5Target: 17Links: 29
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
7591
Core Entity Id
64411
Source Entity Count
1
Preferred Name
Hydroxykynureninuria
Name Cn
羟犬尿氨酸尿症
Name Pinyin
Qiang Quan Niao An Suan Niao Zheng
Name En
Hydroxykynureninuria
Name Latin
Bilingual Status
complete
Disease Type
phenotype
Umls Disease Type
Disease or Syndrome
Disgenet Type
phenotype
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
Hydroxykynureninuria
Role
preferred
Name
KYNURENINASE DEFICIENCY
Role
alias
Name
XANTHURENIC ACIDURIA
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS006325
Omim
236800
Umls
C0268474
Sym Map
SMDE03905
Dis Ge Net
C0268474
Umls Sty
T047
Me Sh Class
C16C18
Etcm Disease
Hydroxykynureninuria
Tcmbank Disease
15045
Itcmdb Generated
ITX-DISEASE-702AB9BECB58

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Hydroxykynureninuria Details page
Disease Type
phenotype
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Hydroxykynureninuria
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Muscle diseases;Nephrological diseases;Neuronal diseases
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
phenotype
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or Syndrome