DiseaseID 9898

着色性干皮病变异型

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: 9Target: 12Links: 21
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Record Fields

Scalar fields from the final disease record.

Disease Id
9898
Core Entity Id
67033
Source Entity Count
1
Preferred Name
Xeroderma Pigmentosum, Variant Form
Name Cn
着色性干皮病变异型
Name Pinyin
Zhuo Se Xing Gan Pi Bing Bian Yi Xing
Name En
Xeroderma Pigmentosum, Variant Form
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome; Congenital Abnormality
Disgenet Type
disease
Mesh Class
Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases
Do Class
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue 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
Xeroderma Pigmentosum, Variant Form
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS009444
Sym Map
SMDE14409
Dis Ge Net
C0432328
Umls Sty
T019T047
Me Sh Class
C04C16C17C18
Tcmbank Disease
20352

Attributes

Merged source attributes and domain-specific metadata.

Version
v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome; Congenital Abnormality
Me Sh Disease Class
Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Umls Semantic Type Name
Disease or Syndrome; Congenital Abnormality