Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 11Target: 3Links: 14
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 8888
- Core Entity Id
- 65883
- Source Entity Count
- 1
- Preferred Name
- Carnitine-Acylcarnitine Translocase Deficiency
- Name Cn
- 肉碱-酰基肉碱转位酶缺乏症
- Name Pinyin
- Rou Jian - Xian Ji Rou Jian Zhuan Wei Mei Que Fa Zheng
- Name En
- Carnitine-Acylcarnitine Translocase 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,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Carnitine-Acylcarnitine Translocase Deficiency
Role
preferred
Name
CACT DEFICIENCY
Role
alias
Name
CACTD
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS008077
Omim
212138
Umls
C0342791
Sym Map
SMDE00266
Dis Ge Net
C0342791
Umls Sty
T047
Me Sh Class
C16C18
Tcmbank Disease
29633
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
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