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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 
22q11.2 deletion syndrome +  
acquired immunodeficiency +  
acute graft vs. host disease  
Adamantinomatous Craniopharyngioma 
adrenal gland disease +   
aggressive insulitis 
alpha thalassemia-intellectual disability syndrome type 1 
alpha-thalassemia-myelodysplastic syndrome 
anemia +   
autoimmune disease +   
autoimmune disorder of blood +   
autoimmune disorder of endocrine system +   
autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis 
autosomal dominant familial periodic fever 
autosomal recessive osteopetrosis 7 
Bamforth-Lazarus syndrome 
benign insulitis 
beta thalassemia +  
blepharophimosis - intellectual disability syndrome, SBBYS type 
blood coagulation disease +   
blood disease +   
blood group incompatibility +  
blood platelet disease +   
Bloom syndrome 
bone marrow disorder +   
campomelic dysplasia 
cerebral toxoplasmosis 
choledocholithiasis 
combined partial 17-alpha-hydroxylase/17,20-lyase deficiency 
congenital hematological disorder +  
congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome 
congenital toxoplasmosis 
cryopyrin-associated periodic syndrome +  
deafness-lymphedema-leukemia syndrome 
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome 
disorder of GNAS inactivation +  
disorders of vitamin D metabolism +  
duplication of the pituitary gland 
endocrine neoplasm +   
endocrine tuberculosis +  
epidermodysplasia verruciformis +  
erythrocyte disorder +   
erythroderma desquamativum 
familial hypocalciuric hypercalcemia +  
familial Mediterranean fever +  
female athlete triad syndrome 
Follicular Variant Thyroid Gland Papillary Carcinoma 
GATA1-Related X-Linked Cytopenia +  
Genetic endocrine tumor +   
genito-palato-cardiac syndrome 
geotrichosis 
gonadal disorder +   
graft versus host disease +   
Granulomatosis with Polyangiitis +   
growth hormone insensitivity with immune dysregulation 1, autosomal recessive 
Hematological disorder with renal involvement +  
hematological toxicity 
hematopoietic and lymphoid system neoplasm +   
hemorrhagic disease +   
hereditary endocrine growth disease +  
Histiocytic and Dendritic Cell Neoplasm +  
hyperamylasemia 
hyperimmunoglobulinemia D with periodic fever 
hyperinsulinemic hypoglycemia +  
hypersensitivity reaction disease +   
hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome 
hypoinsulinemic hypoglycemia and body hemihypertrophy 
hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism 
immune deficiency disease +   
immune system cancer +   
immune system organ benign neoplasm +  
immune system toxicity  
immunodeficiency disease +   
immunodeficiency-related disorder +  
immunoproliferative disorder 
infantile-onset periodic fever-panniculitis-dermatosis syndrome 
inherited obesity +  
L-ferritin deficiency 
leukocyte disorder +   
Leydig cell hypoplasia +  
Leydig Cell Tumor +  
liver disease +   
lymphangitis 
lymphoid system disorder +   
Melkersson-Rosenthal syndrome 
Mixed Somatotroph-Lactotroph Pituitary Gland Adenoma 
monoclonal gammopathy +   
multiple chemical sensitivity 
muscular pseudohypertrophy-hypothyroidism syndrome 
myositis +   
Neoplastic Medium-Sized B-Lymphocyte with Basophilic Cytoplasm 
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 
paraneoplastic hematological syndrome +  
parathyroid disease +   
parneoplastic endocrine syndrome +  
phagocytic cell dysfunction +  
pituitary deficiency +  
pituitary gland disease +   
polycystic ovary syndrome  
polyendocrinopathy +  
Poorly Differentiated Thyroid Gland Carcinoma +  
premalignant hematological system disease +   
proteosome-associated autoinflammatory syndrome +  
psoriasis +   
pyogenic arthritis-pyoderma gangrenosum-acne syndrome 
rag2 deficiency 
rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome 
Rare genetic endocrine disease +   
Rare genetic hematologic disease +  
Rare genetic immune disease +  
Roifman syndrome 
Schnitzler syndrome 
splenic disease +   
spondyloarthropathy +   
T-cell large granular lymphocyte leukemia 
thrombocytopenic purpura +  
thymus gland disorder +  
A non-neoplastic or neoplastic disorder that affects the thymus. Representative examples include thymic hyperplasia, thymoma, and thymic carcinoma.
thymus hyperplasia 
thyroid disease +   
Thyroid Gland Mucosa-Associated Lymphoid Tissue Lymphoma 
Thyroid Gland Oncocytic Follicular Carcinoma 
thyroid hormone metabolism, abnormal +  
transcobalamin II deficiency 
twin-to-twin transfusion syndrome 
type II hypersensitivity reaction disease +   
Vici syndrome 
Wolfram-like syndrome 
 thymus neoplasm +  

Synonyms
Exact Synonyms: DOID:533 ;   NCIT:C26962 ;   disease of thymus ;   disease of thymus gland ;   disease or disorder of thymus ;   disorder of thymus ;   disorder of thymus gland ;   http://identifiers.org/medgen/57585 ;   http://identifiers.org/snomedct/20673009 ;   http://linkedlifedata.com/resource/umls/id/C0154199
Related Synonyms: thymus disorder
Alternate IDs: MONDO:0003393
Xrefs: DOID:533 ;   ICD9:254 ;   ICD9:254.9 ;   MEDGEN:57585 ;   NCI:C26962 ;   SCTID:20673009 ;   UMLS:C0154199
External Ontologys: disease_has_location EFO:UBERON:0002370
Definition Sources: NCIT:C26962

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