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Term:
Parent Terms Term With Siblings Child Terms
acromegaly 
Disorder of bile acid synthesis +  
Disorder of phospholipids, sphingolipids and fatty acids biosynthesis with central nervous system predominant involvement +  
Disorder of phospholipids, sphingolipids and fatty acids biosynthesis with peripheral nerves predominant involvement +  
Disorder of phospholipids, sphingolipids and fatty acids biosynthesis with skeletal muscle predominant involvement +  
Familial partial lipodystrophy due to AKT2 mutations 
Familial partial lipodystrophy, Köbberling type 
Genetic disorder of sex development +  
Genetic obesity +  
Genetic polyendocrinopathy +  
glycosylphosphatidylinositol biosynthesis defect 21 
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 +   
X-linked dominant chondrodysplasia punctata 

Synonyms
Xrefs: ICD10:E78.0 ;   ICD10:E78.1 ;   ICD10:E78.2 ;   ICD10:E78.3 ;   ICD10:E78.4 ;   ICD10:E78.5 ;   ICD10:E78.6 ;   ICD10:E78.8 ;   ICD10:E78.9

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