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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
17,20-lyase deficiency, isolated 
17-alpha-hydroxylase/17,20-lyase deficiency, combined complete 
17-alpha-hydroxylase/17,20-lyase deficiency, combined partial 
Adamantinomatous Craniopharyngioma 
adrenal gland disease +   
aromatase excess syndrome 
autoimmune disorder of endocrine system +   
Bamforth-Lazarus syndrome 
Bartholin gland disease 
beta thalassemia +  
blepharophimosis - intellectual disability syndrome, SBBYS type 
campomelic dysplasia 
choledocholithiasis 
classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency +  
combined partial 17-alpha-hydroxylase/17,20-lyase 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 
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome 
disorder of GNAS inactivation +  
disorders of vitamin D metabolism +  
double uterus-hemivagina-renal agenesis syndrome 
duplication of the pituitary gland 
dysplasia of cervix +   
endocrine neoplasm +   
endocrine tuberculosis +  
familial hypocalciuric hypercalcemia +  
female athlete triad syndrome 
female genital tuberculosis 
female reproductive system disease +   
Follicular Variant Thyroid Gland Papillary Carcinoma 
Genetic endocrine tumor +   
genito-palato-cardiac syndrome 
gonadal disorder +   
A non-neoplastic or neoplastic disorder that affects the testis or the ovary.
habitual abortion 
hand-foot-genital syndrome 
hereditary endocrine growth disease +  
hyperinsulinemic hypoglycemia +  
hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome 
hypoinsulinemic hypoglycemia and body hemihypertrophy 
hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism 
hypospadias  
infertility +   
inherited obesity +  
Leydig cell hypoplasia +  
Leydig Cell Tumor +  
liver disease +   
male reproductive system disease +   
Mixed Somatotroph-Lactotroph Pituitary Gland Adenoma 
mullerian duct anomalies-limb anomalies syndrome 
muscular pseudohypertrophy-hypothyroidism syndrome 
neuroendocrine disorder +  
NKX2-1 related choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunction +  
Non-Neoplastic Bile Duct Disorder +   
pancreas disease +   
Papillary Craniopharyngioma 
Papillary Tumor of the Pineal Region 
parathyroid disease +   
parneoplastic endocrine syndrome +  
pelvic organ prolapse +   
physiological sexual disorder +   
pituitary deficiency +  
pituitary dwarfism +  
pituitary gland disease +   
polycystic ovary syndrome  
polyendocrinopathy +  
Poorly Differentiated Thyroid Gland Carcinoma +  
rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome 
Rare genetic endocrine disease +   
reproductive system neoplasm +   
sexually transmitted disease +   
spondylocostal dysostosis-anal and genitourinary malformations syndrome 
thymus gland disorder +  
thymus hyperplasia 
thyroid disease +   
Thyroid Gland Mucosa-Associated Lymphoid Tissue Lymphoma 
Thyroid Gland Oncocytic Follicular Carcinoma 
thyroid hormone metabolism, abnormal +  
Wolfram-like syndrome 

Synonyms
Exact Synonyms: disease of gonad ;   disease or disorder of gonad ;   disorder of gonad ;   disorder of gonads ;   gonad disease ;   gonad disease or disorder ;   gonadal disorders
Alternate IDs: MONDO:0002259
Xrefs: DOID:2277 ;   MEDGEN:9074 ;   MESH:D006058 ;   NCI:C26786 ;   UMLS:C0018050
External Ontologys: disease_has_location EFO:UBERON:0000991
Definition Sources: NCIT:P378

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