|
congenital lipoatrophic diabetes
|
10020 |
|
|
X inactivation, familial skewed
|
100209 |
|
|
BSCL2-related Brunzell syndrome
|
10020 |
|
|
BSCL2 congenital generalized lipodystrophy (disease)
|
10020 |
|
|
lipodystrophy, congenital generalized, type 2
|
10020 |
|
|
lipodystrophy, congenital generalized, type 2; CGL2
|
http://purl.obolibrary.org/obo/MONDO_0010020 |
|
|
parainfluenza 1 infection
|
100203 |
|
|
congenital generalized lipodystrophy (disease) caused by mutation in BSCL2
|
10020 |
|
|
Berardinelli-Seip congenital lipodystrophy type 2
|
10020 |
|
|
congenital generalized lipodystrophy type 2
|
10020 |
|
|
Berardinelli-Seip congenital lipodystrophy, type 2
|
10020 |
|
|
necrosis, aseptic, of bone
|
D010020 |
|
