DiseaseID 16062

先天性谷氨酰胺缺乏症

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: 1Formula: 12Symptom: 5Target: 17Links: 41
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Record Fields

Scalar fields from the final disease record.

Disease Id
16062
Core Entity Id
74082
Source Entity Count
1
Preferred Name
Glutamine Deficiency, Congenital
Name Cn
先天性谷氨酰胺缺乏症
Name Pinyin
Xian Tian Xing Gu An Xian An Que Fa Zheng
Name En
Glutamine Deficiency, Congenital
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
v1,v2
Suppressed
No

Names

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

Name
Glutamine Deficiency, Congenital
Role
preferred
Name
GLUTAMINE SYNTHASE DEFICIENCY, CONGENITAL SYSTEMIC
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS018154
Omim
610015
Umls
C1864910
Sym Map
SMDE01908
Dis Ge Net
C1864910
Umls Sty
T047
Me Sh Class
C16C18
Etcm Disease
Glutamine Deficiency, Congenital
Tcmbank Disease
7398
Itcmdb Generated
ITX-DISEASE-A8270BFC4944

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Glutamine Deficiency, Congenital Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Glutamine Deficiency, Congenital
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Nephrological diseases;Neuronal diseases
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