Abnormality of the uterus
Symptom Information:
Symptom ID: | HPO:0000130 | |||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): | ||||||||||||||||||||||||||||
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) Abnormal internal genitalia(HPO:0000812) Abnormality of female internal genitalia(HPO:0000008) Abnormality of the uterus(HPO:0000130) MedDRA: 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) |
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Database Frequency: | 86 / 7739 | |||||||||||||||||||||||||||
Resource: |
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-Küster-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) |
OVARIAN DYSGENESIS 2 | (OMIM:300510) |
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) |
WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME | (OMIM:194072) |
Waardenburg syndrome | (Orphanet:3440) |