DiseaseID 16454

酪氨酸激酶2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: 1Links: 1
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Record Fields

Scalar fields from the final disease record.

Disease Id
16454
Core Entity Id
74531
Source Entity Count
1
Preferred Name
Tyrosine Kinase 2 Deficiency
Name Cn
酪氨酸激酶2缺乏症
Name Pinyin
Lao An Suan Ji Mei 2 Que Fa Zheng
Name En
Tyrosine Kinase 2 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; Hemic and Lymphatic Diseases
Do Class
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
Hpo Class Name
Do Class Name
Disease Definition
Version
Suppressed

Names

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

Name
Tyrosine Kinase 2 Deficiency
Role
preferred
Name
Immunodeficiency 35
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS018730
Omim
611521
Dis Ge Net
C1969086
Umls Sty
T047
Me Sh Class
C15C16C20
Tcmbank Disease
26004

Attributes

Merged source attributes and domain-specific metadata.

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