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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
familial partial lipodystrophy type 1 
familial partial lipodystrophy type 2  
familial partial lipodystrophy type 3  
familial partial lipodystrophy type 4  
familial partial lipodystrophy type 5  
familial partial lipodystrophy type 6  
Familial Partial Lipodystrophy Type 7  
Familial Partial Lipodystrophy Type 8  
An autosomal dominant disorder characterized by abnormal distribution of subcutaneous adipose tissue. Caused by heterozygous mutation in the ADRA2A gene on chromosome 10q25.
Familial Partial Lipodystrophy Type 9  

Synonyms
Exact Synonyms: FPLD8 ;   LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 8
Primary IDs: OMIM:620679
Definition Sources: OMIM:620679

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