Uterine neoplasm
Symptom Information:
Symptom ID: | HPO:0010784 | ||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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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 genital system(HPO:0000078) Abnormal genital system morphology(HPO:0012243) Abnormality of the female genitalia(HPO:0010460) Abnormality of female internal genitalia(HPO:0000008) Abnormality of the uterus(HPO:0000130) Uterine neoplasm(HPO:0010784) Abnormal internal genitalia(HPO:0000812) Abnormality of female internal genitalia(HPO:0000008) Abnormality of the uterus(HPO:0000130) Uterine neoplasm(HPO:0010784) Genital neoplasm(HPO:0010787) Uterine neoplasm(HPO:0010784) Neoplasm of the genitourinary tract(HPO:0007379) Genital neoplasm(HPO:0010787) Uterine neoplasm(HPO:0010784) Neoplasm(HPO:0002664) Neoplasm by anatomical site(HPO:0011793) Neoplasm of the genitourinary tract(HPO:0007379) Genital neoplasm(HPO:0010787) Uterine neoplasm(HPO:0010784) MedDRA: Reproductive system and breast disorders(MedDRA:10038604) Uterine, pelvic and broad ligament disorders(MedDRA:10046828) Uterine neoplasm(HPO:0010784) |
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Database Frequency: | 13 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Alport syndrome | (Orphanet:63) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
Carney complex | (Orphanet:1359) |
Cowden syndrome | (Orphanet:201) |
Familial leiomyomatosis | (Orphanet:523) |
Hereditary nonpolyposis colon cancer | (Orphanet:144) |
Invasive mole | (Orphanet:99925) |
KERATOSIS, FAMILIAL ACTINIC | (OMIM:148390) |
Muir-Torre syndrome | (Orphanet:587) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
PTEN hamartoma tumor syndrome | (Orphanet:306498) |
Peutz-Jeghers syndrome | (Orphanet:2869) |
Placental site trophoblastic tumor | (Orphanet:99928) |