Polycystic ovaries-urethral sphincter dysfunction syndrome

Polycystic ovaries-urethral sphincter dysfunction syndrome is characterised by urinary retention and incomplete emptying of the bladder associated with abnormal electromyographic activity. It has been described in 33 women, 14 of whom also had polycystic ovaries.



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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)		 PMID
(PMCID)
        

Phenotype(s) retrieved from Orphanet

    Total: 12

HPO ID Term Frequency
HP:0000147 Polycystic ovaries Frequent (79-30%)
HP:0000795 Abnormality of the urethra Frequent (79-30%)
HP:0003457 EMG abnormality Frequent (79-30%)
HP:0100518 Dysuria Frequent (79-30%)
HP:0000016 Urinary retention Occasional (29-5%)
HP:0000876 Oligomenorrhea Occasional (29-5%)
HP:0001007 Hirsutism Occasional (29-5%)
HP:0001061 Acne Occasional (29-5%)
HP:0000020 Urinary incontinence Very rare (4-1%)
HP:0000132 Menorrhagia Very rare (4-1%)
HP:0000137 Abnormality of the ovary Very rare (4-1%)
HP:0000141 Amenorrhea Very rare (4-1%)


Phenotype(s) retrieved from case reports

    Total: 0

HPO ID Term # of case reports


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID