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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 +   
autoimmune disorder of endocrine system +   
Bamforth-Lazarus syndrome 
beta thalassemia +  
blepharophimosis - intellectual disability syndrome, SBBYS type 
campomelic dysplasia 
choledocholithiasis 
combined partial 17-alpha-hydroxylase/17,20-lyase deficiency 
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome 
disorder of GNAS inactivation +  
disorders of vitamin D metabolism +  
duplication of the pituitary gland 
endocrine neoplasm +   
endocrine tuberculosis +  
familial hypocalciuric hypercalcemia +  
female athlete triad syndrome 
Follicular Variant Thyroid Gland Papillary Carcinoma 
Genetic endocrine tumor +   
genito-palato-cardiac syndrome 
gonadal disorder +   
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 
inherited obesity +  
Leydig cell hypoplasia +  
Leydig Cell Tumor +  
liver disease +   
Mixed Somatotroph-Lactotroph Pituitary Gland Adenoma 
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 +  
pituitary deficiency +  
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 +   
thymus gland disorder +  
thymus hyperplasia 
thyroid disease +   
A disease involving the thyroid gland.
Thyroid Gland Mucosa-Associated Lymphoid Tissue Lymphoma 
Thyroid Gland Oncocytic Follicular Carcinoma 
thyroid hormone metabolism, abnormal +  
Wolfram-like syndrome 

Synonyms
Exact Synonyms: DOID:50 ;   NCIT:C26893 ;   Thyroiditis ;   disease of thyroid gland ;   disease or disorder of thyroid gland ;   disorder of thyroid gland ;   http://identifiers.org/medgen/1378579 ;   http://identifiers.org/mesh/D013959 ;   http://identifiers.org/snomedct/14304000 ;   http://linkedlifedata.com/resource/umls/id/C4317107
Xrefs: DOID:50 ;   ICD10:E06 ;   ICD10:E07 ;   ICD10CM:E00-E07 ;   ICD9:240-246.99 ;   ICD9:246.8 ;   ICD9:246.9 ;   MEDGEN:1378579 ;   MESH:D013959 ;   MONDO:0003240
External Ontologys: disease_has_location EFO:UBERON:0002046
Definition Sources: https://orcid.org/0000-0002-6601-2165

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