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.
CACP
|
8828 |
|
PTORCH2
|
18828 |
|
USP18 deficiency
|
18828 |
|
UPS18 deficiency
|
18828.0 |
|
CACP syndrome
|
8828 |
|
Jacobs syndrome
|
8828 |
|
PAC syndrome
|
8828 |
|
arthropathy-camptodactyly syndrome
|
8828 |
|
camptodactyly-arthropathy-coxa-vara-pericarditis syndrome
|
8828 |
|
camptodactyly-arthropathy-pericarditis syndrome
|
8828 |
|
pericarditis-arthropathy-camptodactyly syndrome
|
8828 |
|
Cortico-basal degeneration
|
D000088282 |
|
pseudo-TORCH syndrome 2
|
18828 |
|
pseudo-TORCH syndrome 2; PTORCH2
|
http://purl.obolibrary.org/obo/MONDO_0018828 |
|
pericarditis arthropathy camptodactyly syndrome
|
8828 |
|