3-Beta-hydroxy-Delta-5-C27-steroid oxidoreductase deficiency
|
0011906 |
|
laminin alpha-2 deficiency
|
0011925 |
|
mannosyltransferase 2 deficiency
|
0011933 |
|
glucosyltransferase 2 deficiency
|
0011969 |
|
congenital heart defects, multiple types, with Cardiac rhythm and conduction disturbances
|
0013988 |
|
neural tube defects, susceptibility to
|
0008449 |
|
heart septal defects, ventricular
|
0002070 |
|
lymphedema-atrial septal defects-facial changes syndrome
|
0011166 |
|
splenogonadal fusion-limb defects-micrognathia syndrome
|
0008460 |
|
distichiasis-congenital heart defects-peripheral vascular anomalies syndrome
|
0007465 |
|
long bone deficiencies associated with cleft lip-palate
|
0009997 |
|