DiseaseID 14166

家族性CD8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: 1Herb: 1Symptom: 1Target: 17Links: 26
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Record Fields

Scalar fields from the final disease record.

Disease Id
14166
Core Entity Id
71912
Source Entity Count
1
Preferred Name
Cd8 Deficiency, Familial
Name Cn
家族性CD8缺乏症
Name Pinyin
Jia Zu Xing Cd8 Que Fa Zheng
Name En
Cd8 Deficiency, Familial
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
Cd8 Deficiency, Familial
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS015517
Omim
608957
Umls
C1837065
Sym Map
SMDE02097
Dis Ge Net
C1837065
Umls Sty
T047
Me Sh Class
C16C20
Etcm Disease
Cd8 Deficiency, Familial
Tcmbank Disease
29083
Itcmdb Generated
ITX-DISEASE-CA6DCA0BC1F9

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Cd8 Deficiency, Familial Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Cd8 Deficiency, Familial
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood 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