| 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.
|
paternal del(14)(q32.2)
|
16780 |
|
|
disease, heartwater
|
6780 |
|
|
heartwater disease
|
6780 |
|
|
familial, 8 atrial fibrillation
|
C567802 |
|
|
paternal monosomy 14q32.2
|
16780 |
|
|
GSD IXC
|
C567809 |
|
|
malaria, vivax
|
D016780 |
|
|
plasmodium vivax malaria
|
D016780 |
|
|
hereditary polymorphic light eruption
|
C566780 |
|
|
glycogen storage disease IXC
|
C567809 |
|
|
polymorphic light eruption, hereditary
|
C566780 |
|
|
primary t-cell immunodeficiency disorders
|
C536780 |
|
|
t cell immunodeficiency primary
|
C536780 |
|
|
combined, 1 pituitary hormone deficiency
|
C567803 |
|
|
paternal 14q32.2 microdeletion syndrome
|
16780 |
|
