DiseaseID 25800
胱硫醚β-合成酶缺乏所致同型半胱氨酸尿症
Homocystinuria Due To Cystathionine Beta-Synthase Deficiency
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 1Herb: 1Symptom: 6Target: 15Links: 32
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 25800
- Core Entity Id
- 118368
- Source Entity Count
- 1
- Preferred Name
- Homocystinuria Due To Cystathionine Beta-Synthase Deficiency
- Name Cn
- 胱硫醚β-合成酶缺乏所致同型半胱氨酸尿症
- Name Pinyin
- Guang Liu Mi Β- He Cheng Mei Que Fa Suo Zhi Tong Xing Ban Guang An Suan Niao Zheng
- Name En
- Homocystinuria Due To Cystathionine Beta-Synthase Deficiency
- 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
Homocystinuria Due To Cystathionine Beta-Synthase Deficiency
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C3150344
Sym Map
SMDE00405
Etcm Disease
Homocystinuria Due to Cystathionine Beta-Synthase Deficiency
Itcmdb Generated
ITX-DISEASE-B97CAA01B9E2
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Homocystinuria Due to Cystathionine Beta-Synthase Deficiency Details page
Basic Information
Disease Name
Homocystinuria Due to Cystathionine Beta-Synthase Deficiency
Global Category
Fetal diseases;Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Eye diseases;Neuronal diseases