Polycystic ovaries
Symptom Information:
Symptom ID: | HPO:0000147 | ||||||||||||||||
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 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 ovary(HPO:0000137) Ovarian cyst(HPO:0000138) Polycystic ovaries(HPO:0000147) Abnormal internal genitalia(HPO:0000812) Abnormality of female internal genitalia(HPO:0000008) Abnormality of the ovary(HPO:0000137) Ovarian cyst(HPO:0000138) Polycystic ovaries(HPO:0000147) MedDRA: Reproductive system and breast disorders(MedDRA:10038604) Ovarian and fallopian tube disorders(MedDRA:10033283) Ovarian and fallopian tube cysts and neoplasms(MedDRA:10033121) Polycystic ovaries(HPO:0000147) |
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Database Frequency: | 18 / 7739 | ||||||||||||||||
Resource: |
All diseases associated with this symptom:
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS | (OMIM:201750) |
Alström syndrome | (Orphanet:64) |
Bangstad syndrome | (Orphanet:1227) |
Bardet-Biedl syndrome | (Orphanet:110) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
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) |
HEPATIC ADENOMAS, FAMILIAL | (OMIM:142330) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 | (OMIM:608594) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 | (OMIM:269700) |
Leprechaunism | (Orphanet:508) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Polycystic ovaries - urethral sphincter dysfunction | (Orphanet:2795) |
Proteus-like syndrome | (Orphanet:2969) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism | (Orphanet:3085) |