DiseaseID 29037
遗传性Wilms瘤（WT1）
Hereditary Wilms' Tumor (Wt1)
NCI2016_02D:Familial embryonal neoplasm derived from nephrogenic blastemal cells. Several lines of differentiation, including blastemal, stromal and epithelial, are usually expressed. Comprises approximately 1% of Wilms
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Disease: 1Symptom: 1Target: 12Links: 13
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 29037
- Core Entity Id
- 121605
- Source Entity Count
- 1
- Preferred Name
- Hereditary Wilms' Tumor (Wt1)
- Name Cn
- 遗传性Wilms瘤（WT1）
- Name Pinyin
- Yi Chuan Xing Wilms Liu （wt1）
- Name En
- Hereditary Wilms' Tumor (Wt1)
- 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:Familial embryonal neoplasm derived from nephrogenic blastemal cells. Several lines of differentiation, including blastemal, stromal and epithelial, are usually expressed. Comprises approximately 1% of Wilms tumors. (AFIP fascicle version 2.0)
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hereditary Wilms' Tumor (Wt1)
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C0677779
Sym Map
SMDE09438
Itcmdb Generated
ITX-DISEASE-9919ADCB9338
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Definition
NCI2016_02D:Familial embryonal neoplasm derived from nephrogenic blastemal cells. Several lines of differentiation, including blastemal, stromal and epithelial, are usually expressed. Comprises approximately 1% of Wilms tumors. (AFIP fascicle version 2.0)