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
Arranging relationship network...
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