nephroblastoma (Cancer)
Information
- Disease name
- nephroblastoma
- Disease ID
- DOID:2154
- Description
- "A kidney cancer that affects the kidneys and typically located_in children." [url:http\://en.wikipedia.org/wiki/Wilms%27_tumor]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes | Mutation | Description | Source | Links |
---|
NCT ID | Status | Phase | Summary | Start date | Completion date |
---|---|---|---|---|---|
NCT00001509 | Completed | Phase 2 | A Phase II Trial of All-Trans-Retinoic Acid in Combination With Interferon-Alpha 2a in Children With Recurrent Neuroblastoma or Wilms' Tumor | July 1996 | May 2000 |
NCT05245123 | Completed | Psychosocial Situation of Children With Rare Solid Abdominal Tumors and Their Families | February 21, 2022 | March 31, 2023 | |
NCT04423484 | Recruiting | Therapeutic Recommendations for Nephroblastoma | July 1, 2020 | September 30, 2026 | |
NCT05985161 | Recruiting | Phase 2 | A Study of Selinexor in People With Wilms Tumors and Other Solid Tumors | August 1, 2023 | August 1, 2029 |
NCT04168788 | Unknown status | N/A | Pharmacogenetic Study of Antimitotic Therapies Involved in Hepatic VOD in Children With Nephroblastoma or ALL | January 1, 2020 | January 1, 2022 |
- Disase is a (Disease Ontology)
- DOID:263
- Cross Reference ID (Disease Ontology)
- ICDO:8960/3
- Cross Reference ID (Disease Ontology)
- MESH:D009396
- Cross Reference ID (Disease Ontology)
- MIM:194070
- Cross Reference ID (Disease Ontology)
- NCI:C27730
- Cross Reference ID (Disease Ontology)
- NCI:C3267
- Cross Reference ID (Disease Ontology)
- NCI:C6180
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:25081006
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0027708
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C1332219
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C1333015
- Exact Synonym (Disease Ontology)
- adult nephroblastoma
- Disase Synonym (Disease Ontology)
- Wilms' tumor
- HPO alt_id (Human Phenotype Ontology)
- HP:0000115
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0002667
- OrphaNumber from OrphaNet (Orphanet)
- 654