DiseaseID 7619

乙酰辅酶A羧化酶缺乏症

disease

Back to Browse

Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

Click a node to open it in a new tab
Disease: 1Symptom: 1Target: 1Links: 2
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
7619
Core Entity Id
64444
Source Entity Count
1
Preferred Name
Acetyl-Coa: Carboxylase Deficiency
Name Cn
乙酰辅酶A羧化酶缺乏症
Name Pinyin
Yi Xian Fu Mei A Suo Hua Mei Que Fa Zheng
Name En
Acetyl-Coa: Carboxylase 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
v1
Suppressed
No

Names

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

Name
Acetyl-Coa: Carboxylase Deficiency
Role
preferred
Name
Acetyl-Coa Carboxylase Deficiency
Role
preferred
Name
ACACA DEFICIENCY
Role
alias
Name
ACACAD
Role
alias
Name
ACC1 DEFICIENCY
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS006374
Omim
613933
Umls
C0268603
Sym Map
SMDE04611
Dis Ge Net
C0268603
Umls Sty
T047
Me Sh Class
C16C18
Tcmbank Disease
27516

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
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