Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 6Symptom: 6Target: 17Links: 36
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 25836
- Core Entity Id
- 118404
- Source Entity Count
- 1
- Preferred Name
- Hyperphenylalaninemia, Bh4-Deficient, C
- Name Cn
- 高苯丙氨酸血症，BH4缺乏，C型
- Name Pinyin
- Gao Ben Bing An Suan Xue Zheng ，bh4 Que Fa ，c Xing
- Name En
- Hyperphenylalaninemia, Bh4-Deficient, C
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hyperphenylalaninemia, Bh4-Deficient, C
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C0268465
Sym Map
SMDE00551
Etcm Disease
Hyperphenylalaninemia, Bh4-Deficient, C
Itcmdb Generated
ITX-DISEASE-ECA83338E517
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Hyperphenylalaninemia, Bh4-Deficient, C Details page
Basic Information
Disease Name
Hyperphenylalaninemia, Bh4-Deficient, C
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Neuronal diseases