Send us a Message

Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Parent Terms Term With Siblings Child Terms
adrenal gland disease +   
alopecia, neurologic defects, and endocrinopathy syndrome  
autoimmune disease of endocrine system +   
Bardet-Biedl syndrome +   
diabetes mellitus +   
Dwarfism +   
Endocrine Bone Diseases +   
endocrine gland cancer +   
Endocrine Gland Neoplasms +   
Endocrine Tuberculosis 
endocrine-cerebro-osteodysplasia syndrome  
Estrogen Resistance  
Female Athlete Triad Syndrome 
gonadal disease +   
hypothalamic neoplasm +   
Hypothalamic Obesity +  
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease 1  
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease 2  
Laurence-Moon syndrome  
liver disease +   
Macrosomia Adiposa Congenita 
Microgastria Limb Reduction Defect 
Pallister-Hall-like Syndrome  
pancreas disease +   
parathyroid gland disease +   
pituitary gland disease +   
Disorders involving either the ADENOHYPOPHYSIS or the NEUROHYPOPHYSIS. These diseases usually manifest as hypersecretion or hyposecretion of PITUITARY HORMONES. Neoplastic pituitary masses can also cause compression of the OPTIC CHIASM and other adjacent structures.
Polyendocrine-Polyneuropathy Syndrome  
proprotein convertase 1/3 deficiency  
Retinohepatoendocrinologic Syndrome 
thymus gland disease +   
thyroid gland disease +   

Exact Synonyms: Adenohypophyseal Disease ;   Adenohypophyseal Diseases ;   Anterior Pituitary Disease ;   Anterior Pituitary Diseases ;   Hypophyseal Disorder ;   Hypophyseal Disorders ;   Neurohypophyseal Disease ;   Neurohypophyseal Diseases ;   Pituitary Disease ;   Pituitary Diseases ;   Pituitary Disorder ;   Pituitary Disorders ;   Pituitary Gland Diseases ;   Posterior Pituitary Disease ;   Posterior Pituitary Diseases
Primary IDs: MESH:D010900 ;   RDO:0005351
Xrefs: ICD9CM:253.1
Definition Sources: "DO" "DO", MESH:D010900

paths to the root