DiseaseID 17744

MASP2缺乏症

disease

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Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

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Disease: 1Target: 18Links: 24
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Record Fields

Scalar fields from the final disease record.

Disease Id
17744
Core Entity Id
76030
Source Entity Count
1
Preferred Name
Masp2 Deficiency
Name Cn
MASP2缺乏症
Name Pinyin
Masp2 Que Fa Zheng
Name En
Masp2 Deficiency
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
Masp2 Deficiency
Role
preferred
Name
LCAPD2
Role
alias
Name
LECTIN COMPLEMENT ACTIVATION PATHWAY, DEFECT IN, 2
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS020765
Omim
613791
Umls
C3151085
Sym Map
SMDE03536
Dis Ge Net
C3151085
Umls Sty
T047
Me Sh Class
C16C20
Etcm Disease
Masp2 Deficiency
Tcmbank Disease
29376
Itcmdb Generated
ITX-DISEASE-36AC46BD9012

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Masp2 Deficiency Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Masp2 Deficiency
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Immune diseases
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