Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 3Target: 6Links: 9
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 13470
- Core Entity Id
- 71114
- Source Entity Count
- 1
- Preferred Name
- Pseudo-Zellweger Syndrome
- Name Cn
- 假性泽尔韦格综合征
- Name Pinyin
- Jia Xing Ze Er Wei Ge Zong He Zheng
- Name En
- Pseudo-Zellweger Syndrome
- 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 DiseasesFemale Urogenital Diseases and Pregnancy Complications; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Digestive System Diseases; Male Urogenital Diseases
- Do Class
- genetic disease
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
- Hpo Class Name
- Do Class Name
- genetic disease
- Disease Definition
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Pseudo-Zellweger Syndrome
Role
preferred
Name
Deficiency of Acetyl-Coa Acetyltransferase
Role
preferred
Name
3-Ketothiolase Deficiency
Role
alias
Name
Alpha-Methylacetoacetic Aciduria
Role
alias
Name
Alpha-Methylacetoaceticaciduria
Role
alias
Name
Beta-Ketothiolase Deficiency
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS014499HBDIS014528
Omim
203750
Umls
C1533628
Sym Map
SMDE12511
Do Class
DOID:630
Dis Ge Net
C1533628C1536500
Umls Sty
T047
Me Sh Class
C06C10C12C13C16C18
Tcmbank Disease
1128123457
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
genetic disease
Disease Type
disease
Do Disease Class
genetic disease
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic DiseasesFemale Urogenital Diseases and Pregnancy Complications; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Digestive System Diseases; Male Urogenital Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or Syndrome