DiseaseID 7608

高氨血症III型

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: 3Links: 3
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Record Fields

Scalar fields from the final disease record.

Disease Id
7608
Core Entity Id
64431
Source Entity Count
1
Preferred Name
Hyperammonemia, Type Iii
Name Cn
高氨血症III型
Name Pinyin
Gao An Xue Zheng Iii Xing
Name En
Hyperammonemia, Type Iii
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Nervous System Diseases; 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; Nervous System Diseases
Hpo Class Name
Do Class Name
Disease Definition
Version
Suppressed

Names

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

Name
Hyperammonemia, Type Iii
Role
preferred
Name
N-Acetyl Glutamate Synthetase Deficiency
Role
alias
Name
N-Acetylglutamate Synthase Deficiency
Role
alias
Name
N-Acetylglutamate Synthetase Deficiency
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS006349
Omim
237310
Dis Ge Net
C0268543
Umls Sty
T047
Me Sh Class
C10C16C18
Tcmbank Disease
7316

Attributes

Merged source attributes and domain-specific metadata.

Disease Type
disease
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Nervous System Diseases; 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; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome