Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Herb: 12Target: 17Links: 36
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 7565
- Core Entity Id
- 64380
- Source Entity Count
- 1
- Preferred Name
- Apnea, Postanesthetic
- Name Cn
- 麻醉后呼吸暂停
- Name Pinyin
- Ma Zui Hou Hu Xi Zan Ting
- Name En
- Apnea, Postanesthetic
- 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; Nutritional and Metabolic DiseasesRespiratory Tract Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Respiratory Tract Diseases
- Hpo Class Name
- Do Class Name
- Disease Definition
- Version
- Suppressed
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Apnea, Postanesthetic
Role
preferred
Name
Butyrylcholinesterase Deficiency
Role
preferred
Name
Butyrylcholinesterase Deficiency, Fluoride-Resistant, Japanese Type
Role
preferred
Name
Pseudocholinesterase Deficiency
Role
preferred
Name
Suxamethonium Sensitivity
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS006283HBDIS013203HBDIS014665HBDIS018386HBDIS018387
Omim
617936
Dis Ge Net
C0268379C1283400C1622434C1867468C1867469
Umls Sty
T046T047
Me Sh Class
C08C16C18C23
Etcm Disease
Butyrylcholinesterase Deficiency
Tcmbank Disease
11273126672859969308719
Itcmdb Generated
ITX-DISEASE-637F08109109
Attributes
Merged source attributes and domain-specific metadata.
Page Title
Disease Butyrylcholinesterase Deficiency Details page
Disease Type
diseasephenotype
Umls Disease Type
Disease or SyndromePathologic Function
Basic Information
Disease Name
Butyrylcholinesterase Deficiency
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Liver diseases;Neuronal diseases;Respiratory diseases
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic DiseasesRespiratory Tract Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Respiratory Tract Diseases
Umls Semantic Type Name
Disease or SyndromePathologic Function