| 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.
|
cortex disorder, auditory
|
D001304 |
|
|
cortex disorders, auditory
|
D001304 |
|
|
dysfunction, central auditory
|
D001304 |
|
|
dysfunctions, central auditory
|
D001304 |
|
|
congenital disorder of glycosylation type 1o
|
13049 |
|
|
familial cerebral cavernous malformation caused by mutation in CCM2
|
11304 |
|
|
CCM2 familial cerebral cavernous malformation
|
11304 |
|
|
spastic quadriplegic cerebral palsy 3
|
13048 |
|
|
lactate dehydrogenase deficiency type A
|
13047 |
|
|
glycogen storage disease caused by mutation in LDHA
|
13047 |
|
|
glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
|
13047 |
|
|
glycogen storage disease due to muscle beta-enolase deficiency
|
13046 |
|
|
glycogen storage disease type 11
|
13047 |
|
|
glycogen storage disease type 13
|
13046 |
|
|
hypertensive renal disease, benign
|
1304 |
|
