Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 1Target: 12Links: 13
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 13841
- Core Entity Id
- 71537
- Source Entity Count
- 2
- Preferred Name
- Peroxisome Biogenesis Disorders
- Name Cn
- 过氧化物酶体生物合成障碍
- Name Pinyin
- Guo Yang Hua Wu Mei Ti Sheng Wu He Cheng Zhang Ai
- Name En
- Peroxisome Biogenesis Disorders
- Name Latin
- Bilingual Status
- complete
- Disease Type
- group
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- group
- 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
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Peroxisome Biogenesis Disorders
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS015036
Umls
C1832200
Icd10
E71.51
Sym Map
SMDE12103
Dis Ge Net
C1832200
Umls Sty
T047
Me Sh Class
C16C18
Tcmbank Disease
158613970
Itcmdb Generated
ITX-DISEASE-4F5A9B9A6EF9
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
group
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
group
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or Syndrome