DiseaseID 8891

肌苷三磷酸酶缺乏症

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
8891
Core Entity Id
65886
Source Entity Count
1
Preferred Name
Inosine Triphosphatase Deficiency
Name Cn
肌苷三磷酸酶缺乏症
Name Pinyin
Ji Gan San Lin Suan Mei Que Fa Zheng
Name En
Inosine Triphosphatase 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
Suppressed

Names

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

Name
Inosine Triphosphatase Deficiency
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS008080
Omim
613850
Dis Ge Net
C0342800
Umls Sty
T047
Me Sh Class
C16C18
Tcmbank Disease
16976

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