Nephroblastoma

Symptom Information:

Symptom ID: HPO:0002667
Synonyms:
Nephroblastoma [HPO:0002667]
Wilm's tumor [HPO:0002667]
Wilms tumor [HPO:0002667]
Nephroblastoma [Orphanet:50550]
Nephroblastoma (disorder) [Orphanet:50550]
Nephroblastoma (morphologic abnormality) [Orphanet:50550]
Nephroblastoma [OMIM:Nephroblastoma]
Nephroblastoma (Wilms tumor) [OMIM:Nephroblastoma (Wilms tumor)]
Wilms tumor [OMIM:Wilms tumor]
Nephroblastoma/Wilms tumor [Orphanet:50550]
Nephroblastoma [MedDRA:10029145]
Wilms tumor [MedDRA:10029145]
Wilms tumour [MedDRA:10029145]
Wilms' tumor [MedDRA:10029145]
Quality:
Cross references:
Orphanet:50550 "Nephroblastoma/Wilms tumor" [Orphanet:50550]
OMIM: "Nephroblastoma" [OMIM:Nephroblastoma]
OMIM: "Nephroblastoma (Wilms tumor)" [OMIM:Nephroblastoma (Wilms tumor)]
OMIM: "Wilms tumor" [OMIM:Wilms tumor]
UMLS:C0027708 "Nephroblastoma" [HPO:0002667]
UMLS:C0027708 "Nephroblastoma" [Orphanet:50550]
Is a (Direct Parents):
HPO         Embryonal renal neoplasm
HPO         Embryonal neoplasm
MedDRA Renal neoplasms malignant
Orphanet Renal neoplasm
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Neoplasm of the genitourinary tract(HPO:0007379)
             Urinary tract neoplasm(HPO:0010786)
                Renal neoplasm(HPO:0009726)
                   Embryonal renal neoplasm(HPO:0011794)
                      Nephroblastoma(HPO:0002667)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Renal neoplasm(HPO:0009726)
                      Embryonal renal neoplasm(HPO:0011794)
                         Nephroblastoma(HPO:0002667)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the genitourinary tract(HPO:0007379)
                Urinary tract neoplasm(HPO:0010786)
                   Renal neoplasm(HPO:0009726)
                      Embryonal renal neoplasm(HPO:0011794)
                         Nephroblastoma(HPO:0002667)
          Neoplasm by histology(HPO:0011792)
             Embryonal neoplasm(HPO:0002898)
                Nephroblastoma(HPO:0002667)
MedDRA:
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Renal and urinary tract neoplasms malignant and unspecified(MedDRA:10038364)
       Renal neoplasms malignant(MedDRA:10068208)
          Nephroblastoma(HPO:0002667)
Database Frequency: 30 / 7739
Resource:

All diseases associated with this symptom:

2q37 microdeletion syndrome (Orphanet:1001)
Beckwith-Wiedemann syndrome (Orphanet:116)
Beckwith-Wiedemann syndrome due to 11p15 microdeletion (Orphanet:231127)
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 (Orphanet:231117)
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 (Orphanet:96193)
Denys-Drash syndrome (Orphanet:220)
FANCONI ANEMIA, COMPLEMENTATION GROUP N (OMIM:610832)
Familial idiopathic steroid-resistant nephrotic syndrome (Orphanet:656)
Hemihypertrophy (Orphanet:2128)
Hyperparathyroidism - jaw tumor syndrome (Orphanet:99880)
LI-FRAUMENI SYNDROME 1 (OMIM:151623)
Li-Fraumeni syndrome (Orphanet:524)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 (OMIM:257300)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Mulibrey nanism (Orphanet:2576)
Nephroblastoma (Orphanet:654)
Perlman syndrome (Orphanet:2849)
SILVER-RUSSELL SYNDROME (OMIM:180860)
SOTOS SYNDROME 1 (OMIM:117550)
Silver-Russell syndrome (Orphanet:813)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Sotos syndrome (Orphanet:821)
WAGR syndrome (Orphanet:893)
WILMS TUMOR 1 (OMIM:194070)
WILMS TUMOR 2 (OMIM:194071)
WILMS TUMOR 3 (OMIM:194090)
WILMS TUMOR 4 (OMIM:601363)
WILMS TUMOR 5 (OMIM:601583)
WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME (OMIM:194072)