| 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.
|
Direct Hyperbilirubinemia
|
DISO:NCI_NICHD |
|
|
Osteogenesis Imperfecta Type III
|
DISO:NCI_NICHD |
|
|
Hypophosphatasia
|
DISO:NCI_NICHD |
|
|
Pseudohypoaldosteronism Type 1
|
DISO:NCI_NICHD |
|
|
Gordon Syndrome
|
DISO:NCI_NICHD |
|
|
Pseudohypoaldosteronism Type 2
|
DISO:NCI_NICHD |
|
|
Gitelman Syndrome
|
DISO:NCI_NICHD |
|
|
Carbamoyl Phosphate Synthetase Deficiency
|
DISO:NCI_NICHD |
|
|
Methylmalonic Acidemia
|
DISO:NCI_NICHD |
|
|
Glutaric Aciduria, Type 2
|
DISO:NCI_NICHD |
|
|
Methylcrotonyl-CoA Carboxylase Deficiency
|
DISO:NCI_NICHD |
|
|
Arakawa Syndrome II
|
DISO:NCI_NICHD |
|
|
Methionine Synthase Deficiency
|
DISO:NCI_NICHD |
|
|
Tetrahydrofolate Methyltransferase Deficiency
|
DISO:NCI_NICHD |
|
|
5,10-Methylenetetrahydrofolate Reductase Deficiency
|
DISO:NCI_NICHD |
|