DiseaseID 11766
无白蛋白血症
phenotype
NCI2016_02D:A rare, autosomal recessive inherited disorder characterized by the absence or severe reduction of circulating human serum albumin.
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 9Symptom: 1Target: 18Links: 34
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 11766
- Core Entity Id
- 69191
- Source Entity Count
- 1
- Preferred Name
- Analbuminemia
- Name Cn
- 无白蛋白血症
- Name Pinyin
- Wu Bai Dan Bai Xue Zheng
- Name En
- Analbuminemia
- Name Latin
- Bilingual Status
- complete
- Disease Type
- phenotype
- Umls Disease Type
- Finding
- Disgenet Type
- phenotype
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- NCI2016_02D:A rare, autosomal recessive inherited disorder characterized by the absence or severe reduction of circulating human serum albumin.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Analbuminemia
Role
preferred
Name
ANALBA
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS012340
Omim
616000
Umls
C0878666
Sym Map
SMDE01116
Dis Ge Net
C0878666
Umls Sty
T033
Etcm Disease
Analbuminemia
Tcmbank Disease
26615
Itcmdb Generated
ITX-DISEASE-454E9BF1B02D
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Analbuminemia Details page
Disease Type
phenotype
Umls Disease Type
Finding
Basic Information
Disease Name
Analbuminemia
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Bone diseases
Disease Definition
NCI2016_02D:A rare, autosomal recessive inherited disorder characterized by the absence or severe reduction of circulating human serum albumin.
Dis Ge Net Disease Type
phenotype
Umls Semantic Type Name
Finding