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Term:
Rare genetic hypothalamic or pituitary disease (EFO:Orphanet:183628)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0) Naked Mole-rat: (0) Green Monkey: (0)
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 +  
Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency 
Lipodystrophy - intellectual disability - deafness 
Non-acquired premature ovarian failure +  
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 +   

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