| manager |
|
| language |
- |
| license |
- |
| created at |
2017-12-21 11:07:44 UTC |
| updated at |
2017-12-22 12:31:05 UTC |
|
2 layers
|
520,470 entries
|
There is 0 pattern entry.
|
Defect, Patent or persistent, foramen ovale
|
DISO:MTHICD9 |
|
|
Defect, fossa ovalis
|
DISO:MTHICD9 |
|
|
Defect, Patent or persistent, ostium secundum
|
DISO:MTHICD9 |
|
|
Supracristal ventricular septal defect
|
DISO:MTH |
|
|
Anomaly NOS of vena cava
|
DISO:MTHICD9 |
|
|
Congenital failure of fusion
|
DISO:MTH |
|
|
Cerebrooculofacioskeletal Syndrome 1
|
DISO:MTH |
|
|
Multiple pterygium syndrome
|
DISO:MTH |
|
|
Thrombocytopenia-Absent Radius Syndrome
|
DISO:MTH |
|
|
Thrombocytopenia with absent radii (TAR) syndrome
|
DISO:MTHICD9 |
|
|
Achondrogenesis type 1A
|
DISO:MTH |
|
|
Achondrogenesis, type IB (disorder)
|
DISO:MTH |
|
|
Diastrophic dysplasia
|
DISO:MTH |
|
|
Acromicric Dysplasia
|
DISO:MTH |
|
|
Frontometaphyseal dysplasia
|
DISO:MTH |
|
