DiseaseID 17005

MYD88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: 15Links: 24
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Record Fields

Scalar fields from the final disease record.

Disease Id
17005
Core Entity Id
75163
Source Entity Count
1
Preferred Name
Myd88 Deficiency
Name Cn
MYD88缺乏症
Name Pinyin
Myd88 Que Fa Zheng
Name En
Myd88 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
Suppressed

Names

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

Name
Myd88 Deficiency
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS019475
Omim
612260
Dis Ge Net
C2677092
Umls Sty
T047
Me Sh Class
C16C20
Etcm Disease
Myd88 Deficiency
Tcmbank Disease
24939
Itcmdb Generated
ITX-DISEASE-2BDADACDEAF4

Attributes

Merged source attributes and domain-specific metadata.

Page Title
Disease Myd88 Deficiency Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Myd88 Deficiency
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Immune diseases;Neuronal 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