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
- 15356
- Core Entity Id
- 73280
- Source Entity Count
- 1
- Preferred Name
- Laron Syndrome Type 2
- Name Cn
- 拉伦综合征2型
- Name Pinyin
- La Lun Zong He Zheng 2 Xing
- Name En
- Laron Syndrome Type 2
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Endocrine System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine 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
Laron Syndrome Type 2
Role
preferred
Name
Growth Hormone Insensitivity With Immunodeficiency
Role
alias
Name
Laron Syndrome Due To Postreceptor Defect
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS017169
Omim
245590
Dis Ge Net
C1855548
Umls Sty
T047
Me Sh Class
C05C16C19
Tcmbank Disease
32344
Attributes
Merged source attributes and domain-specific metadata.
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Endocrine System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
Umls Semantic Type Name
Disease or Syndrome