DiseaseID 17754

纤维胶凝蛋白3缺乏症

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: 1Formula: 4Herb: 1Target: 18Links: 29
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
17754
Core Entity Id
76042
Source Entity Count
1
Preferred Name
Ficolin 3 Deficiency
Name Cn
纤维胶凝蛋白3缺乏症
Name Pinyin
Xian Wei Jiao Ning Dan Bai 3 Que Fa Zheng
Name En
Ficolin 3 Deficiency
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Do Class
Hpo Class
Mesh Class Name
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
Ficolin 3 Deficiency
Role
preferred
Name
FCN3 DEFICIENCY
Role
alias
Name
LCAPD3
Role
alias
Name
LECTIN COMPLEMENT ACTIVATION PATHWAY, DEFECT IN, 3
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS020791
Omim
613860
Umls
C3151226
Sym Map
SMDE01613
Dis Ge Net
C3151226
Umls Sty
T047
Etcm Disease
Ficolin 3 Deficiency
Tcmbank Disease
1328
Itcmdb Generated
ITX-DISEASE-6F4DDE86FD95

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Ficolin 3 Deficiency Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Ficolin 3 Deficiency
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Immune diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome