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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
abortion +  
amenorrhea 
bacterial sexually transmitted disease +   
Bartholin duct cyst 
Central precocious puberty +   
Complex Endometrial Hyperplasia 
delayed puberty, self-limited 
dysplasia of cervix +   
Endometrial Hyperplasia without Atypia 
fallopian tube disease +  
female genital tract fistula 
female genital tract polyp +   
female genital tuberculosis 
female infertility +   
female reproductive system neoplasm +   
Genetic disorder of sex development of gynecological interest +  
genetic non-acquired premature ovarian failure 
Gynatresia 
high-risk pregnancy  
Hyperandrogenism due to cortisone reductase deficiency 
mammary-digital-nail syndrome 
menopausal or post-menopausal disease 
menstrual cycle-dependent periodic fever 
mullerian aplasia +  
Müllerian aplasia +  
ovarian disease +   
Pelvic Inflammatory Disease +  
polyp of vulva +  
premenstrual tension 
preterm premature rupture of the membranes  
prolapse of female genital organ +  
Rare disorder with hypogonadotropic hypogonadism +  
Rare genetic female infertility +  
rectocele 
Simple Endometrial Hyperplasia 
Trichomonas vaginitis +  
uterine disorder +   
A non-neoplastic or neoplastic disorder that affects the uterine corpus or the cervix. Representative examples of non-neoplastic disorders include endometritis and cervicitis. Representative examples of neoplastic disorders include endometrial carcinoma, carcinosarcoma, and cervical carcinoma.
Uterine Inertia 
uterine prolapse  
vaginal disorder +  
vulval varices 
vulvar disease +  

Synonyms
Exact Synonyms: DOID:345 ;   NCIT:C26907 ;   disease of uterus ;   disease or disorder of uterus ;   disorder of uterus ;   http://identifiers.org/medgen/22590 ;   http://identifiers.org/mesh/D014591 ;   http://identifiers.org/snomedct/12337004 ;   http://linkedlifedata.com/resource/umls/id/C0042131 ;   uterine disease
Alternate IDs: MONDO:0002654
Xrefs: DOID:345 ;   ICD9:621.8 ;   ICD9:621.9 ;   MEDGEN:22590 ;   MESH:D014591 ;   NCI:C26907 ;   SCTID:12337004 ;   UMLS:C0042131
External Ontologys: disease_has_location EFO:UBERON:0000995
Definition Sources: NCIT:P378

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