DiseaseID 2352

过氧化物酶体生物发生障碍3A型(泽尔韦格)

disease

Back to Browse

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: 3Target: 1Links: 4
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
2352
Core Entity Id
2650
Source Entity Count
1
Preferred Name
Peroxisome Biogenesis Disorder 3A (Zellweger)
Name Cn
过氧化物酶体生物发生障碍3A型(泽尔韦格)
Name Pinyin
Guo Yang Hua Wu Mei Ti Sheng Wu Fa Sheng Zhang Ai 3a Xing ( Ze Er Wei Ge )
Name En
Peroxisome Biogenesis Disorder 3A (Zellweger)
Name Latin
Bilingual Status
complete
Disease Type
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Do Class
genetic disease; disease of metabolism
Hpo Class
Mesh Class Name
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
Peroxisome Biogenesis Disorder 3A (Zellweger)
Role
preferred
Name
Peroxisome Biogenesis Disorder, Complementation Group 3
Role
preferred
Name
CG3
Role
alias
Name
PBD3A
Role
alias
Name
Peroxisome Biogenesis Disorder 3A
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS029038HBDIS029408
Omim
614859
Umls
C1866340C3553929
Sym Map
SMDE02388
Do Class
DOID:0014667DOID:630
Dis Ge Net
C1866340C3553929
Umls Sty
T047
Me Sh Class
C16C18
Itcmdb Generated
ITX-DISEASE-3C5D209FCD4B

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Do Disease Class
genetic disease; disease of metabolism
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