Cystocele

Symptom Information:

Symptom ID: HPO:0100645
Synonyms:
Cystocele (disorder) [Orphanet:37640]
Cystocele [Orphanet:37640]
Cystocele [MedDRA:10011803]
Cystourethrocele [MedDRA:10011803]
Quality:
Cross references:
Orphanet:37640 "Cystocele" [Orphanet:37640]
UMLS:C0010695 "Cystocele" [Orphanet:37640]
Is a (Direct Parents):
MedDRA Pelvic prolapse conditions
HPO         Abnormality of the bladder
Orphanet Bladder and ureter anomalies
HPO         Vaginal hernia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of connective tissue(HPO:0003549)
          Hernia(HPO:0100790)
             Genital hernia(HPO:0100823)
                Vaginal hernia(HPO:0100672)
                   Cystocele(HPO:0100645)
       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 vagina(HPO:0000142)
                         Vaginal hernia(HPO:0100672)
                            Cystocele(HPO:0100645)
                Abnormality of the female genitalia(HPO:0010460)
                   Abnormality of female internal genitalia(HPO:0000008)
                      Abnormality of the vagina(HPO:0000142)
                         Vaginal hernia(HPO:0100672)
                            Cystocele(HPO:0100645)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the lower urinary tract(HPO:0010936)
                Abnormality of the bladder(HPO:0000014)
                   Cystocele(HPO:0100645)
MedDRA:
Reproductive system and breast disorders(MedDRA:10038604)
    Uterine, pelvic and broad ligament disorders(MedDRA:10046828)
       Pelvic prolapse conditions(MedDRA:10062916)
          Cystocele(HPO:0100645)
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)