|
amelogenesis imperfecta, type 1G
|
http://purl.obolibrary.org/obo/MONDO_0008771 |
|
|
amelogenesis imperfecta nephrocalcinosis
|
8771 |
|
|
absent enamel, nephrocalcinosis and apparently normal calcium metabolism
|
8771 |
|
|
congenital anomaly of interventricular communication
|
18771 |
|
|
congenital anomaly of ventricular septum
|
18771 |
|
|
congenital ventricular septal anomaly
|
18771 |
|
|
amelogenesis imperfecta, type IG
|
8771 |
|
|
amelogenesis imperfecta type Ig
|
http://purl.obolibrary.org/obo/MONDO_0008771 |
|
|
amelogenesis imperfecta, type Ig
|
http://purl.obolibrary.org/obo/MONDO_0008771 |
|
|
amelogenesis imperfecta, type Ig; AI1G
|
http://purl.obolibrary.org/obo/MONDO_0008771 |
|
