| 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.
|
Del(2)(q31.1)
|
16652 |
|
|
l-xylulosuria
|
C536652 |
|
|
monosomy 2q31.1
|
16652 |
|
|
HID syndrome
|
C566528 |
|
|
shohat type SEMD
|
C566523 |
|
|
intraventricular septal defect, and deafness brachydactyly
|
C566521 |
|
|
spastic paraplegia and evans syndrome
|
C566652 |
|
|
myocardial infarction, anterior wall
|
6652 |
|
|
myocardial infarction, anterolateral
|
6652 |
|
|
myocardial infarctions, anterolateral
|
6652 |
|
|
myocardial infarction, anteroseptal
|
6652 |
|
|
myocardial infarctions, anteroseptal
|
6652 |
|
|
l-xylulose reductase deficiency
|
C536652 |
|
|
hystrix-like, with deafness ichthyosis
|
C566528 |
|
|
infarction, anterolateral myocardial
|
6652 |
|
