|
velocardiofacial syndrome
|
D004062 |
|
|
deletion syndrome, 22q11.2
|
D004062 |
|
|
familial third and fourth pharyngeal pouch syndrome
|
D004062 |
|
|
conotruncal anomaly face syndrome
|
D004062 |
|
|
conotruncal anomaly face syndrome (CTAF)
|
D004062 |
|
|
velo cardio facial syndrome
|
D004062 |
|
|
third and fourth pharyngeal pouch syndrome
|
D004062 |
|
|
autosomal dominant opitz g bbb syndrome
|
D004062 |
|
|
autosomal dominant opitz g-bbb syndrome
|
D004062 |
|
|
22q11.2 deletion syndrome
|
D004062 |
|
|
deletion 22q11.2 syndrome
|
D004062 |
|
|
pharyngeal pouch syndrome
|
D004062 |
|
|
hypoplasia of thymus and parathyroids
|
D004062 |
|
