DiseaseID 17235

染色体5P13重复综合征

disease

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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: 1Symptom: 4Target: 5Links: 9
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Record Fields

Scalar fields from the final disease record.

Disease Id
17235
Core Entity Id
75435
Source Entity Count
1
Preferred Name
Chromosome 5P13 Duplication Syndrome
Name Cn
染色体5P13重复综合征
Name Pinyin
Ran Se Ti 5p13 Chong Fu Zong He Zheng
Name En
Chromosome 5P13 Duplication Syndrome
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and Symptoms
Do Class
genetic disease
Hpo Class
Mesh Class Name
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Hpo Class Name
Do Class Name
genetic disease
Disease Definition
Version
v2
Suppressed
No

Names

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

Name
Chromosome 5P13 Duplication Syndrome
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS019891
Umls
C2750805
Sym Map
SMDE07146
Do Class
DOID:630
Dis Ge Net
C2750805
Umls Sty
T047
Me Sh Class
C16C23
Tcmbank Disease
3947

Attributes

Merged source attributes and domain-specific metadata.

Version
v2
Suppress
0
Do Class Name
genetic disease
Disease Type
disease
Do Disease Class
genetic disease
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Umls Semantic Type Name
Disease or Syndrome