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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
endocrine system disease +     
hematologic disease +     
hyperplasia +     
immune system disease +     
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 +   
Adrenal Medullary Hyperplasia 
aggressive insulitis 
alpha thalassemia-intellectual disability syndrome type 1 
alpha-thalassemia-myelodysplastic syndrome 
anemia +   
Atypical Endometrial Hyperplasia 
Atypical Lobular Breast Hyperplasia 
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 
benign prostatic hyperplasia  
beta thalassemia +  
blepharophimosis - intellectual disability syndrome, SBBYS type 
blood coagulation disease +   
blood disease +   
blood group incompatibility +  
blood platelet disease +   
Bloom syndrome 
bone marrow disorder +   
C-Cell Hyperplasia 
campomelic dysplasia 
cerebral toxoplasmosis 
choledocholithiasis 
Columnar Cell Hyperplasia of the Breast 
combined partial 17-alpha-hydroxylase/17,20-lyase deficiency 
Complex Endometrial Hyperplasia 
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 +  
Endometrial Hyperplasia without Atypia 
epidermodysplasia verruciformis +  
erythrocyte disorder +   
erythroderma desquamativum 
familial hypocalciuric hypercalcemia +  
familial Mediterranean fever +  
female athlete triad syndrome 
focal epithelial hyperplasia 
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 
immunoproliferative small intestinal disease 
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 +   
neointimal hyperplasia 
Neoplastic Medium-Sized B-Lymphocyte with Basophilic Cytoplasm 
neuroendocrine cell hyperplasia of infancy 
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 +   
Parathyroid Hyperplasia 
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 
Simple Endometrial Hyperplasia 
splenic disease +   
spondyloarthropathy +   
T-cell large granular lymphocyte leukemia 
thrombocytopenic purpura +  
thymus gland disorder +  
thymus hyperplasia 
Enlargement of the thymus. A condition described in the late 1940's and 1950's as pathological thymic hypertrophy was status thymolymphaticus and was treated with radiotherapy. Unnecessary removal of the thymus was also practiced. It later became apparent that the thymus undergoes normal physiological hypertrophy, reaching a maximum at puberty and involuting thereafter. The concept of status thymolymphaticus has been abandoned. Thymus hyperplasia is present in two thirds of all patients with myasthenia gravis. (From Segen, Dictionary of Modern Medicine, 1992; Cecil Textbook of Medicine, 19th ed, p1486)
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 +   
urothelial hyperplasia +  
Usual Ductal Breast Hyperplasia 
Vici syndrome 
Wolfram-like syndrome 

Synonyms
Xrefs: DOID:9004911 ;   MeSH:D013952

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