Ovarian neoplasm
Symptom Information:
Symptom ID: | HPO:0100615 | |||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||||||||
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) Neoplasm(HPO:0002664) Neoplasm by anatomical site(HPO:0011793) Neoplasm of the genitourinary tract(HPO:0007379) Genital neoplasm(HPO:0010787) Gonadal neoplasm(HPO:0010785) Ovarian neoplasm(HPO:0100615) Abnormality of the genitourinary system(HPO:0000119) Neoplasm of the genitourinary tract(HPO:0007379) Genital neoplasm(HPO:0010787) Gonadal neoplasm(HPO:0010785) Ovarian neoplasm(HPO:0100615) Abnormality of the genital system(HPO:0000078) Abnormal genital system morphology(HPO:0012243) Abnormal internal genitalia(HPO:0000812) Abnormality of female internal genitalia(HPO:0000008) Abnormality of the ovary(HPO:0000137) Ovarian neoplasm(HPO:0100615) Abnormality of the female genitalia(HPO:0010460) Abnormality of female internal genitalia(HPO:0000008) Abnormality of the ovary(HPO:0000137) Ovarian neoplasm(HPO:0100615) Genital neoplasm(HPO:0010787) Gonadal neoplasm(HPO:0010785) Ovarian neoplasm(HPO:0100615) MedDRA: Reproductive system and breast disorders(MedDRA:10038604) Ovarian and fallopian tube disorders(MedDRA:10033283) Ovarian and fallopian tube cysts and neoplasms(MedDRA:10033121) Ovarian neoplasm(HPO:0100615) |
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Database Frequency: | 25 / 7739 | |||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
46,XY partial gonadal dysgenesis | (Orphanet:251510) |
Acquired hypertrichosis lanuginosa | (Orphanet:2221) |
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4 | (OMIM:614337) |
Carney complex | (Orphanet:1359) |
Cowden syndrome | (Orphanet:201) |
Dermatomyositis | (Orphanet:221) |
Desmoplastic small round cell tumor | (Orphanet:83469) |
Enchondromatosis | (Orphanet:296) |
Gorlin syndrome | (Orphanet:377) |
Hereditary nonpolyposis colon cancer | (Orphanet:144) |
Lhermitte-Duclos disease | (Orphanet:65285) |
Maffucci syndrome | (Orphanet:163634) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Muir-Torre syndrome | (Orphanet:587) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Peutz-Jeghers syndrome | (Orphanet:2869) |
Polymyositis | (Orphanet:732) |
Primary peritoneal carcinoma | (Orphanet:168829) |
Proteus syndrome | (Orphanet:744) |
Proteus-like syndrome | (Orphanet:2969) |
Pseudomyxoma peritonei | (Orphanet:26790) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Schöpf-Schulz-Passarge syndrome | (Orphanet:50944) |
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus | (Orphanet:137608) |
Werner syndrome | (Orphanet:902) |