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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
adrenal gland disease +   
alopecia, neurologic defects, and endocrinopathy syndrome  
autoimmune disease of endocrine system +   
diabetes mellitus +   
A glucose metabolism disease characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both. (DO)
Dwarfism +   
Endocrine Bone Diseases +   
endocrine gland cancer +   
Endocrine Gland Neoplasms +   
Endocrine Tuberculosis 
endocrine-cerebro-osteodysplasia syndrome  
Estrogen Resistance  
Female Athlete Triad Syndrome 
Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency 
Glycosuria +   
gonadal disease +   
hyperglycemia +   
hyperinsulinism +   
hypoglycemia +   
Hypoinsulinemia  
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease  
liver disease +   
Macrosomia Adiposa Congenita 
Microcephaly, Short Stature, and Impaired Glucose Metabolism +   
pancreas disease +   
parathyroid gland disease +   
phosphoglycerate kinase 1 deficiency  
pituitary gland disease +   
Polyendocrine-Polyneuropathy Syndrome  
prediabetes syndrome  
proprotein convertase 1/3 deficiency  
Retinohepatoendocrinologic Syndrome 
SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION  
thymus gland disease +   
thyroid gland disease +   
triosephosphate isomerase deficiency  

Synonyms
Narrow Synonyms: monogenic diabetes ;   transient neonatal diabetes
Primary IDs: MESH:D003920
Xrefs: ICD10CM:E08-E13 ;   ICD9CM:250 ;   NCI:C2985
Definition Sources: http://www.who.int/diabetes/action_online/basics/en/ "DO", https://en.wikipedia.org/wiki/Diabetes_mellitus "DO", https://www.ncbi.nlm.nih.gov/pubmed/9686693 "DO"

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