|
megarbane-dagher-melki type chondrodysplasia
|
C567644 |
|
|
lipodystrophy, berardinelli-seip congenital, type 4, with muscular dystrophy
|
C567642 |
|
|
miyoshi muscular dystrophy 2
|
C567646 |
|
|
miyoshi muscular dystrophy 3
|
C567645 |
|
|
combined immunodeficiency, facial dysmorphism, optic nerve atrophy, skeletal anomalies, and developmental delay
|
C567641 |
|
|
plasminogen activator inhibitor-1 deficiency
|
C567640 |
|
|
berardinelli-seip congenital lipodystrophy, type 4, with muscular dystrophy
|
C567642 |
|
|
Fungi infectious meningitis
|
6764 |
|
|
isolated pure microphthalmia
|
16764 |
|
|
facial dysmorphism, optic nerve atrophy, skeletal anomalies, and developmental delay combined immunodeficiency
|
C567641 |
|
|
isolated anophthalmia-microphthalmia syndrome
|
16764 |
|
|
nonsyndromic anophthalmia-microphthalmia syndrome
|
16764 |
|
|
hyperfibrinolysis due to pai1 deficiency
|
C567640 |
|
|
chondrodysplasia, megarbane-dagher-melki type
|
C567644 |
|
|
congenital generalized, type 4 lipodystrophy
|
C567642 |
|
