Nephroblastoma
Symptom Information:
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) |