Send us a Message



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

Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
acromegaly 
Familial partial lipodystrophy due to AKT2 mutations 
Familial partial lipodystrophy, Köbberling type 
Genetic disorder of sex development +  
Genetic obesity +  
Genetic polyendocrinopathy +  
Hemihypertrophy 
Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency 
Klippel-Trénaunay syndrome 
Lipodystrophy - intellectual disability - deafness 
Non-acquired premature ovarian failure +  
Overgrowth - macrocephaly - facial dysmorphism 
pik3ca related overgrowth spectrum 
Rare disorder with hypergonadotropic hypogonadism +  
Rare dyslipidemia +   
Rare genetic adrenal disease +   
Rare genetic diabetes mellitus +  
Rare genetic hypothalamic or pituitary disease +  
Rare genetic parathyroid disease and phosphocalcic metabolism disorder +  
Rare genetic thyroid disease +   

Synonyms
Xrefs: ICD10:E66.8

paths to the root