DiseaseID 8795

家族性白蛋白异常性高甲状腺素血症

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: 2Links: 2
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Record Fields

Scalar fields from the final disease record.

Disease Id
8795
Core Entity Id
65778
Source Entity Count
1
Preferred Name
Hyperthyroxinemia, Familial Dysalbuminemic
Name Cn
家族性白蛋白异常性高甲状腺素血症
Name Pinyin
Jia Zu Xing Bai Dan Bai Yi Chang Xing Gao Jia Zhuang Xian Su Xue Zheng
Name En
Hyperthyroxinemia, Familial Dysalbuminemic
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases
Do Class
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; 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
Hyperthyroxinemia, Familial Dysalbuminemic
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS007948
Me Sh
D050010
Omim
615999
Dis Ge Net
C0342185
Umls Sty
T047
Me Sh Class
C16C19
Tcmbank Disease
27433

Attributes

Merged source attributes and domain-specific metadata.

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