DiseaseID 26854
48,XXXY综合征
48, Xxxy Syndrome
NCI2016_02D:A rare sex chromosome abnormality in which a male child has 2 extra X chromosomes.
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Herb: 1Symptom: 6Target: 33Links: 41
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26854
- Core Entity Id
- 119422
- Source Entity Count
- 1
- Preferred Name
- 48, Xxxy Syndrome
- Name Cn
- 48,XXXY综合征
- Name Pinyin
- 48,xxxy Zong He Zheng
- Name En
- 48, Xxxy Syndrome
- 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
- NCI2016_02D:A rare sex chromosome abnormality in which a male child has 2 extra X chromosomes.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
48, Xxxy Syndrome
Role
preferred
Name
48,xxxy Syndrome
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C0265498
Sym Map
SMDE05253
Etcm Disease
48,xxxy Syndrome
Itcmdb Generated
ITX-DISEASE-E258029337E9ITX-DISEASE-E4FF2C0B028F
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Page Title
Disease 48,xxxy Syndrome Details page
Basic Information
Disease Name
48,xxxy Syndrome
Global Category
Fetal diseases;Rare diseases
Anatomical Category
Endocrine diseases;Neuronal diseases;Reproductive diseases
Disease Definition
NCI2016_02D:A rare sex chromosome abnormality in which a male child has 2 extra X chromosomes.