| manager |
|
| language |
- |
| license |
- |
| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
|
MONDO_bioport_pref_name
|
183,974 entries
|
There is 0 pattern entry.
|
optic atrophy 7
|
C567833 |
|
|
Heart-hand syndrome 2
|
C536784 |
|
|
spastic quadriplegic, 2 cerebral palsy
|
C567867 |
|
|
paroxysmal familial, 2 ventricular fibrillation
|
C567841 |
|
|
CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT
|
26782 |
|
|
chondrodysplasia punctata 2, X-linked dominant
|
26782 |
|
|
T-cell lymphoma 1a
|
C536782 |
|
|
familial febrile, 3a convulsions
|
C567820 |
|
|
familial febrile, 3a seizures
|
C567820 |
|
|
brachydactyly type A5
|
19678 |
|
|
brachydactyly type A5 nail dysplasia
|
19678 |
|
|
classical hydatidiform Mole
|
16785 |
|
|
fuchs endothelial, 3 corneal dystrophy
|
C567678 |
|
|
chromosome 2P25.3 Duplication syndrome
|
14678 |
|
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 71
|
32678 |
|
