Abnormality of the uterus

Symptom Information:

Symptom ID: HPO:0000130
Uterine abnormalities [HPO:0000130]
Uterine malformations [HPO:0000130]
Uterus anomaly [Orphanet:39140]
Congenital uterine anomaly (disorder) [Orphanet:39140]
Congenital uterine anomaly [Orphanet:39140]
Uterine abnormalities [OMIM:Uterine abnormalities]
Uterine malformations [OMIM:Uterine malformations]
Uterine/uterus/Fallopian tubes anomalies [Orphanet:39140]
Congenital uterine anomaly [MedDRA:10061079]
Bicornuate uterus [MedDRA:10061079]
Bicornuate uterus (pregnancy problem) [MedDRA:10061079]
Congenital abnormalities of uterus complicating pregnancy, childbirth, or the puerperium [MedDRA:10061079]
Congenital abnormalities of uterus, antepartum condition or complication [MedDRA:10061079]
Congenital abnormalities of uterus, delivered, with mention of postpartum complication [MedDRA:10061079]
Congenital abnormalities of uterus, postpartum condition or complication [MedDRA:10061079]
Congenital abnormalities of uterus, unspecified as to episode of care [MedDRA:10061079]
Congenital abnormalities of uterus, with delivery [MedDRA:10061079]
Congenital uterine anomaly NOS [MedDRA:10061079]
Congenital uterine disorder NOS [MedDRA:10061079]
Didelphic uterus [MedDRA:10061079]
Doubling of uterus [MedDRA:10061079]
Other congenital anomalies of uterus [MedDRA:10061079]
Septate uterus [MedDRA:10061079]
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)]
Septate uterus [OMIM:Septate uterus]
Septate uterus (rare) [OMIM:Septate uterus (rare)]
Cross references:
Orphanet:39140 "Uterine/uterus/Fallopian tubes anomalies" [Orphanet:39140]
OMIM: "Uterine abnormalities" [OMIM:Uterine abnormalities]
OMIM: "Uterine malformations" [OMIM:Uterine malformations]
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)]
OMIM: "Septate uterus" [OMIM:Septate uterus]
OMIM: "Septate uterus (rare)" [OMIM:Septate uterus (rare)]
UMLS:C0266383 "Congenital uterine anomaly" [Orphanet:39140]
Is a (Direct Parents):
HPO         Abnormality of female internal genitalia
HPO         Abnormality of the uterine cervix
HPO         Abnormality of the endometrium
MedDRA Female reproductive tract disorders congenital
Orphanet Structural anomalies of the genital system
Is a (Whole tree): HPO:
    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)
                Abnormal internal genitalia(HPO:0000812)
                   Abnormality of female internal genitalia(HPO:0000008)
                      Abnormality of the uterus(HPO:0000130)
Congenital, familial and genetic disorders(MedDRA:10010331)
    Reproductive tract and breast disorders congenital(MedDRA:10038608)
       Female reproductive tract disorders congenital(MedDRA:10016416)
          Abnormality of the uterus(HPO:0000130)
Database Frequency: 86 / 7739

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
46,XX disorder of sex development - anorectal anomalies (Orphanet:2973)
46,XX ovotesticular disorder of sex development (Orphanet:2138)
Acro-renal-mandibular syndrome (Orphanet:958)
Acrofacial dysostosis, Rodriguez type (Orphanet:1788)
Androgen insensitivity syndrome (Orphanet:754)
Autosomal dominant omodysplasia (Orphanet:93328)
Autosomal dominant spondylocostal dysostosis (Orphanet:1797)
Autosomal recessive spondylocostal dysostosis (Orphanet:2311)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bilateral renal agenesis (Orphanet:1848)
CHARGE syndrome (Orphanet:138)
CHILD syndrome (Orphanet:139)
Camptobrachydactyly (Orphanet:1319)
Caudal duplication (Orphanet:1756)
Cloacal exstrophy (Orphanet:93929)
Complete androgen insensitivity syndrome (Orphanet:99429)
Cornelia de Lange syndrome (Orphanet:199)
Cowden syndrome (Orphanet:201)
Craniomicromelic syndrome (Orphanet:1524)
Diabetic embryopathy (Orphanet:1926)
Diaphragmatic defect - limb deficiency - skull defect (Orphanet:2141)
Donnai-Barrow syndrome (Orphanet:2143)
Double uterus - hemivagina - renal agenesis (Orphanet:3411)
Dyskeratosis congenita (Orphanet:1775)
Ehlers-Danlos syndrome due to tenascin-X deficiency (Orphanet:230839)
Ellis Van Creveld syndrome (Orphanet:289)
Familial caudal dysgenesis (Orphanet:1768)
Fanconi anemia (Orphanet:84)
Fraser syndrome (Orphanet:2052)
Fryns syndrome (Orphanet:2059)
Gonadal dysgenesis, XY type - associated anomalies (Orphanet:1770)
Hand-foot-genital syndrome (Orphanet:2438)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hydatidiform mole (Orphanet:99927)
Hydrolethalus (Orphanet:2189)
Hypomandibular faciocranial dysostosis (Orphanet:1790)
Hypoparathyroidism - deafness - renal disease (Orphanet:2237)
Hypoplasminogenemia (Orphanet:722)
Johanson-Blizzard syndrome (Orphanet:2315)
Juvenile polyposis syndrome (Orphanet:2929)
Kallmann syndrome (Orphanet:478)
Lethal chondrodysplasia, Moerman type (Orphanet:1420)
Lethal omphalocele-cleft palate syndrome (Orphanet:2736)
Lymphangioleiomyomatosis (Orphanet:538)
MURCS association (Orphanet:2578)
Matthew-Wood syndrome (Orphanet:2470)
Mayer-Rokitansky-K├╝ster-Hauser syndrome (Orphanet:3109)
Meacham syndrome (Orphanet:3097)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 1 (OMIM:249000)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Mosaic trisomy 9 (Orphanet:99776)
Mullerian duct anomalies - limb anomalies (Orphanet:2491)
Okamoto syndrome (Orphanet:2729)
PAGOD syndrome (Orphanet:991)
PELVIS syndrome (Orphanet:83628)
Partial androgen insensitivity syndrome (Orphanet:90797)
Perrault Syndrome (Orphanet:2855)
Perrault Syndrome 4 (OMIM:615300)
Peters-plus syndrome (Orphanet:709)
Phocomelia, Schinzel type (Orphanet:2879)
Primary hypergonadotropic hypogonadism - partial alopecia (Orphanet:2232)
Prune belly syndrome (Orphanet:2970)
Renal cysts and diabetes syndrome (Orphanet:93111)
Renal-genital-middle ear anomalies (Orphanet:1092)
Rhombencephalosynapsis (Orphanet:59315)
Satoyoshi syndrome (Orphanet:3130)
Short rib-polydactyly syndrome (Orphanet:1505)
Spondylocostal dysostosis - anal and genitourinary malformations (Orphanet:94095)
Syndactyly - telecanthus - anogenital and renal malformations (Orphanet:140952)
Testicular regression syndrome (Orphanet:983)
Thrombocytopenia - absent radius (Orphanet:3320)
Thymic-renal-anal-lung dysplasia (Orphanet:3326)
Townes-Brocks syndrome (Orphanet:857)
Trichodermodysplasia - dental alterations (Orphanet:3353)
Trisomy 13 (Orphanet:3378)
Trisomy 18 (Orphanet:3380)
Ulnar-mammary syndrome (Orphanet:3138)
VACTERL with hydrocephalus (Orphanet:3412)
VACTERL/VATER association (Orphanet:887)
WAGR syndrome (Orphanet:893)
Waardenburg syndrome (Orphanet:3440)