DiseaseID 7618

HMG-CoA裂解酶缺乏症

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: 1Target: 1Links: 1
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
7618
Core Entity Id
64443
Source Entity Count
1
Preferred Name
Hmg Coa Lyase Deficiency
Name Cn
HMG-CoA裂解酶缺乏症
Name Pinyin
Hmg-coa Lie Jie Mei Que Fa Zheng
Name En
Hmg Coa Lyase 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
Suppressed

Names

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

Name
Hmg Coa Lyase Deficiency
Role
preferred
Name
3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency
Role
alias
Name
Hmg-Coa Lyase Deficiency
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS006373
Omim
246450
Dis Ge Net
C0268601
Umls Sty
T047
Me Sh Class
C16C18
Tcmbank Disease
2678

Attributes

Merged source attributes and domain-specific metadata.

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