DiseaseID 17503

17号染色体缺失

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: 8Target: 12Links: 20
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Record Fields

Scalar fields from the final disease record.

Disease Id
17503
Core Entity Id
75745
Source Entity Count
1
Preferred Name
Chromosome 17 Deletion
Name Cn
17号染色体缺失
Name Pinyin
17 Hao Ran Se Ti Que Shi
Name En
Chromosome 17 Deletion
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Cell or Molecular Dysfunction
Disgenet Type
disease
Mesh Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Do Class
Hpo Class
Mesh Class Name
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Hpo Class Name
Do Class Name
Disease Definition
Version
v2
Suppressed
No

Names

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

Name
Chromosome 17 Deletion
Role
preferred
Name
Chromosome 17P Deletion Syndrome
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS020336HBDIS022007
Umls
C3683846
Sym Map
SMDE07123
Dis Ge Net
C2931713C3683846
Umls Sty
T049
Me Sh Class
C10C16C23
Tcmbank Disease
17984298
Itcmdb Generated
ITX-DISEASE-58865EBFA923

Attributes

Merged source attributes and domain-specific metadata.

Version
v2
Suppress
0
Disease Type
diseasephenotype
Umls Disease Type
Cell or Molecular Dysfunction
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Umls Semantic Type Name
Cell or Molecular Dysfunction