Renal neoplasm
Symptom Information:
Symptom ID: | HPO:0009726 | |||||||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the genitourinary system(HPO:0000119) 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) Neoplasm of the genitourinary tract(HPO:0007379) Urinary tract neoplasm(HPO:0010786) Renal neoplasm(HPO:0009726) 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) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Renal neoplasm(HPO:0009726) Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104) Renal and urinary tract neoplasms malignant and unspecified(MedDRA:10038364) Urinary tract neoplasms unspecified malignancy NEC(MedDRA:10046586) Renal neoplasm(HPO:0009726) |
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Database Frequency: | 20 / 7739 | |||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
Birt-Hogg-Dube syndrome | (Orphanet:122) |
Blau syndrome | (Orphanet:90340) |
COWDEN SYNDROME 4 | (OMIM:615107) |
Cowden syndrome | (Orphanet:201) |
Familial leiomyomatosis | (Orphanet:523) |
Gestational trophoblastic neoplasm | (Orphanet:59305) |
Hereditary nonpolyposis colon cancer | (Orphanet:144) |
Invasive mole | (Orphanet:99925) |
Isolated punctate palmoplantar keratoderma | (Orphanet:2338) |
Lymphangioleiomyomatosis | (Orphanet:538) |
Muir-Torre syndrome | (Orphanet:587) |
Nephroblastoma | (Orphanet:654) |
PTEN hamartoma tumor syndrome | (Orphanet:306498) |
Peutz-Jeghers syndrome | (Orphanet:2869) |
Punctate palmoplantar keratoderma type 1 | (Orphanet:79501) |
Rhabdoid tumor | (Orphanet:69077) |
Tuberous sclerosis | (Orphanet:805) |
Von Hippel-Lindau disease | (Orphanet:892) |
Werner syndrome | (Orphanet:902) |