| 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.
|
Gilchrist's disease
|
5672 |
|
|
blastomycotic infection
|
5672 |
|
|
CD79B deficiency
|
C567200 |
|
|
drayer syndrome
|
C567232 |
|
|
adiponectin deficiency
|
C567258 |
|
|
myopia 16
|
C567259 |
|
|
dursun syndrome
|
C567260 |
|
|
1q21.1 deletion
|
C567291 |
|
|
WAGRO syndrome
|
C567292 |
|
|
autosomal dominant 2b deafness
|
C567214 |
|
|
autosomal recessive 1b deafness
|
C567213 |
|
|
1.35-mb chromosome 1q21.1 deletion syndrome
|
C567291 |
|
|
intracranial berry, 10 aneurysm
|
C567237 |
|
|
familial febrile, 10 seizures
|
C567218 |
|
|
autosomal recessive 36, without vestibular involvement deafness
|
C567219 |
|
