| 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.
|
familial isolated dilated cardiomyopathy caused by mutation in NEXN
|
13147 |
|
|
malignant granular cell tumor of skin
|
4314 |
|
|
malignant granular cell tumor of the skin
|
4314 |
|
|
hearing loss, conductive
|
D006314 |
|
|
perisylvian syndrome, congenital bilateral
|
10314 |
|
|
communication disorder, childhood
|
D003147 |
|
|
communication disorders, childhood
|
D003147 |
|
|
AT III deficiency
|
13144 |
|
|
antithrombin 3 deficiency
|
13144 |
|
|
antithrombin III deficiency
|
13144 |
|
|
congenital AT-III deficiency
|
13144 |
|
|
hereditary antithrombin deficiency
|
13144 |
|
|
inherited antithrombin deficiency
|
13144 |
|
|
inflammatory bowel disease, early-onset, autosomal recessive
|
30314 |
|
|
inflammatory bowel disease (infantile ulcerative colitis) 31, autosomal recessive
|
30314 |
|
