Bicornuate uterus

Symptom Information:

Symptom ID: HPO:0000813
Synonyms:
Bicornuate uterus [OMIM:Bicornuate uterus]
Bicornuate uterus (rare) [OMIM:Bicornuate uterus (rare)]
Bicornuate uterus (seen in patients with contiguous gene defect) [OMIM:Bicornuate uterus (seen in patients with contiguous gene defect)]
Quality:
Cross references:
OMIM: "Bicornuate uterus" [OMIM:Bicornuate uterus]
OMIM: "Bicornuate uterus (rare)" [OMIM:Bicornuate uterus (rare)]
OMIM: "Bicornuate uterus (seen in patients with contiguous gene defect)" [OMIM:Bicornuate uterus (seen in patients with contiguous gene defect)]
Is a (Direct Parents):
HPO         Abnormality of the uterus
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 uterus(HPO:0000130)
                         Bicornuate uterus(HPO:0000813)
                Abnormal internal genitalia(HPO:0000812)
                   Abnormality of female internal genitalia(HPO:0000008)
                      Abnormality of the uterus(HPO:0000130)
                         Bicornuate uterus(HPO:0000813)
MedDRA:
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

Acro-renal-mandibular syndrome (Orphanet:958)
Bilateral renal agenesis (Orphanet:1848)
Currarino triad (Orphanet:1552)
Donnai-Barrow syndrome (Orphanet:2143)
Ehlers-Danlos syndrome due to tenascin-X deficiency (Orphanet:230839)
Fraser syndrome (Orphanet:2052)
Fryns syndrome (Orphanet:2059)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Lethal omphalocele-cleft palate syndrome (Orphanet:2736)
MICROPHTHALMIA, SYNDROMIC 12 (OMIM:615524)
MURCS association (Orphanet:2578)
Matthew-Wood syndrome (Orphanet:2470)
Microgastria - limb reduction defect (Orphanet:2538)
Nager syndrome (Orphanet:245)
Perrault Syndrome 4 (OMIM:615300)
ROBERTS SYNDROME (OMIM:268300)
Renal cysts and diabetes syndrome (Orphanet:93111)
Roberts syndrome (Orphanet:3103)
Rudiger syndrome (Orphanet:3118)
Schinzel-Giedion syndrome (Orphanet:798)
Smith-Lemli-Opitz syndrome (Orphanet:818)
UTERINE ANOMALIES (OMIM:192000)