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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
aromatase excess syndrome 
Bartholin gland disease 
classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency +  
congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency 
congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency 
congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency 
congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency 
cortisone reductase deficiency 
Currarino triad 
double uterus-hemivagina-renal agenesis syndrome 
dysplasia of cervix +   
female genital tuberculosis 
female reproductive system disease +   
gonadal disorder +   
habitual abortion 
hand-foot-genital syndrome 
hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism 
hypospadias  
infertility +   
male reproductive system disease +   
A disease involving the male reproductive system.
mullerian duct anomalies-limb anomalies syndrome 
pelvic organ prolapse +   
physiological sexual disorder +   
pituitary dwarfism +  
pituitary gland disease +   
reproductive system neoplasm +   
sexually transmitted disease +   
spondylocostal dysostosis-anal and genitourinary malformations syndrome 

Synonyms
Exact Synonyms: DOID:48 ;   Male reproductive system disorder ;   NCIT:C27019 ;   disease of male reproductive system ;   disease or disorder of male reproductive system ;   disorder of Male reproductive system ;   http://identifiers.org/medgen/66734 ;   http://identifiers.org/mesh/D005832 ;   http://identifiers.org/snomedct/363194005 ;   http://linkedlifedata.com/resource/umls/id/C0236099
Xrefs: DOID:48 ;   ICD10:N40.N51 ;   ICD10:N48 ;   ICD10:N49 ;   ICD10:N50 ;   ICD10:N50.9 ;   ICD10:N51 ;   ICD10CM:N40-N53 ;   ICD10WHO:N40-N51 ;   ICD9:600-608.99
External Ontologys: disease_has_location EFO:UBERON:0000079
Definition Sources: https://orcid.org/0000-0002-6601-2165

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