DiseaseID 14334

备解素缺乏症,II型

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

Record Fields

Scalar fields from the final disease record.

Disease Id
14334
Core Entity Id
72105
Source Entity Count
1
Preferred Name
Properdin Deficiency, Type Ii
Name Cn
备解素缺乏症,II型
Name Pinyin
Bei Jie Su Que Fa Zheng ,ii Xing
Name En
Properdin Deficiency, Type Ii
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Immune System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Do Class
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases
Hpo Class Name
Do Class Name
Disease Definition
Version
v1
Suppressed
No

Names

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

Name
Properdin Deficiency, Type Ii
Role
preferred
Name
Properdin Deficiency, X-Linked
Role
preferred
Name
Properdin Deficiency, Type III
Role
preferred
Name
CFPD
Role
alias
Name
COMPLEMENT FACTOR PROPERDIN DEFICIENCY
Role
alias
Name
PFD
Role
alias
Name
PROPERDIN DEFICIENCY, TYPE I
Role
alias
Name
PROPERDIN P FACTOR DEFICIENCY
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS015756HBDIS015757HBDIS015758
Omim
312060
Umls
C1839454C1839455C1839456
Sym Map
SMDE05069
Dis Ge Net
C1839454C1839455C1839456
Umls Sty
T047
Me Sh Class
C16C20
Tcmbank Disease
192742185224786
Itcmdb Generated
ITX-DISEASE-F110E910893A

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Immune System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases
Umls Semantic Type Name
Disease or Syndrome