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