Urogenital sinus anomaly

Symptom Information:

Symptom ID: HPO:0100779
Synonyms:
Urogenital sinus [Orphanet:39200]
Urogenital sinus [OMIM:Urogenital sinus]
Quality:
Cross references:
Orphanet:39200 "Urogenital sinus" [Orphanet:39200]
OMIM: "Urogenital sinus" [OMIM:Urogenital sinus]
Is a (Direct Parents):
Orphanet Structural anomalies of the genital system
HPO         Abnormality of the urethra
HPO         Abnormality of the vagina
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 vagina(HPO:0000142)
                         Urogenital sinus anomaly(HPO:0100779)
                Abnormal external genitalia(HPO:0000811)
                   Abnormality of male external genitalia(HPO:0000032)
                      Abnormality of the urethra(HPO:0000795)
                         Urogenital sinus anomaly(HPO:0100779)
                Abnormality of the male genitalia(HPO:0010461)
                   Abnormality of male external genitalia(HPO:0000032)
                      Abnormality of the urethra(HPO:0000795)
                         Urogenital sinus anomaly(HPO:0100779)
                Abnormal internal genitalia(HPO:0000812)
                   Abnormality of female internal genitalia(HPO:0000008)
                      Abnormality of the vagina(HPO:0000142)
                         Urogenital sinus anomaly(HPO:0100779)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the lower urinary tract(HPO:0010936)
                Abnormality of the urethra(HPO:0000795)
                   Urogenital sinus anomaly(HPO:0100779)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

46,XX disorder of sex development - anorectal anomalies (Orphanet:2973)
46,XX ovotesticular disorder of sex development (Orphanet:2138)
46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency (Orphanet:753)
McKusick-Kaufman syndrome (Orphanet:2473)
Prune belly syndrome (Orphanet:2970)