Ovarian cyst
Symptom Information:
Symptom ID: | HPO:0000138 | |||||||||||||||
Synonyms: |
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Is a (Direct Parents): | ||||||||||||||||
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) Abnormal internal genitalia(HPO:0000812) Abnormality of female internal genitalia(HPO:0000008) Abnormality of the ovary(HPO:0000137) Ovarian cyst(HPO:0000138) Abnormality of the female genitalia(HPO:0010460) Abnormality of female internal genitalia(HPO:0000008) Abnormality of the ovary(HPO:0000137) Ovarian cyst(HPO:0000138) 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 cyst(HPO:0000138) Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104) Reproductive neoplasms female benign(MedDRA:10038595) Ovarian neoplasms benign(MedDRA:10033273) Ovarian cyst(HPO:0000138) |
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Database Frequency: | 25 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
Alström syndrome | (Orphanet:64) |
Aromatase deficiency | (Orphanet:91) |
Bangstad syndrome | (Orphanet:1227) |
Bardet-Biedl syndrome | (Orphanet:110) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
COWDEN SYNDROME 5 | (OMIM:615108) |
COWDEN SYNDROME 6 | (OMIM:615109) |
Carney complex | (Orphanet:1359) |
Cowden syndrome | (Orphanet:201) |
FRASER-LIKE SYNDROME | (OMIM:229230) |
Familial partial lipodystrophy associated with PPARG mutations | (Orphanet:79083) |
Familial partial lipodystrophy due to AKT2 mutations | (Orphanet:79085) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 | (OMIM:608594) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 | (OMIM:269700) |
Leprechaunism | (Orphanet:508) |
Lhermitte-Duclos disease | (Orphanet:65285) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Peutz-Jeghers syndrome | (Orphanet:2869) |
Polycystic ovaries - urethral sphincter dysfunction | (Orphanet:2795) |
Proteus-like syndrome | (Orphanet:2969) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Rudiger syndrome | (Orphanet:3118) |