Polycystic ovaries

Symptom Information:

Symptom ID: HPO:0000147
Synonyms:
Polycystic ovary [HPO:0000147]
Polycystic ovary disease [HPO:0000147]
Sclerocystic ovaries [HPO:0000147]
Polycystic ovaries (disorder) [Orphanet:39180]
Polycystic Ovary Syndrome [Orphanet:39180]
Polycystic ovaries [OMIM:Polycystic ovaries]
Polycystic ovary [OMIM:Polycystic ovary]
Polycystic ovary disease [OMIM:Polycystic ovary disease]
Sclerocystic ovaries [OMIM:Sclerocystic ovaries]
Abnormal/polycystic ovaries [Orphanet:39180]
Polycystic ovaries [Orphanet:39180]
Polycystic ovaries [MedDRA:10036049]
Polycystic ovary [MedDRA:10036049]
Stein-Leventhal syndrome [MedDRA:10036049]
Polycystic ovarian syndrome [MedDRA:10036049]
Polycystic ovary disease (uncommon) [OMIM:Polycystic ovary disease (uncommon)]
Quality:
Cross references:
HPO:0000138 "Ovarian cysts" [Orphanet:39180]
HPO:0008675 "Enlarged polycystic ovaries" [Orphanet:39180]
Orphanet:39180 "Abnormal/polycystic ovaries" [Orphanet:39180]
OMIM: "Polycystic ovaries" [OMIM:Polycystic ovaries]
OMIM: "Polycystic ovary" [OMIM:Polycystic ovary]
OMIM: "Polycystic ovary disease" [OMIM:Polycystic ovary disease]
OMIM: "Sclerocystic ovaries" [OMIM:Sclerocystic ovaries]
OMIM: "Polycystic ovary disease (uncommon)" [OMIM:Polycystic ovary disease (uncommon)]
UMLS:C0032460 "Polycystic Ovary Syndrome" [Orphanet:39180]
Is a (Direct Parents):
HPO         Ovarian cyst
Orphanet Structural anomalies of the genital system
MedDRA Ovarian and fallopian tube cysts and neoplasms
Orphanet Abnormality of the ovary
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)
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)