DiseaseID 25989

BH4缺乏性高苯丙氨酸血症D型

Hyperphenylalaninemia, Bh4-Deficient, D

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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: 19Links: 24
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
25989
Core Entity Id
118557
Source Entity Count
1
Preferred Name
Hyperphenylalaninemia, Bh4-Deficient, D
Name Cn
BH4缺乏性高苯丙氨酸血症D型
Name Pinyin
Bh4 Que Fa Xing Gao Ben Bing An Suan Xue Zheng D Xing
Name En
Hyperphenylalaninemia, Bh4-Deficient, D
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
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Hyperphenylalaninemia, Bh4-Deficient, D
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Umls
C1849700
Sym Map
SMDE01456
Etcm Disease
Hyperphenylalaninemia, Bh4-Deficient, D
Itcmdb Generated
ITX-DISEASE-06F7DFB1044F

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Hyperphenylalaninemia, Bh4-Deficient, D Details page
Basic Information
Disease Name
Hyperphenylalaninemia, Bh4-Deficient, D
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Neuronal diseases