| 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.
|
Say Carpenter syndrome
|
42902 |
|
|
camptodactyly ichthyosis syndrome
|
8902 |
|
|
uroporphyrinogen 3 synthase deficiency
|
9902 |
|
|
uroporphyrinogen III synthase, deficiency of
|
9902 |
|
|
angioblastoma of the brain stem
|
3902 |
|
|
hemangioblastoma of the brain stem
|
3902 |
|
|
angioblastoma of the brainstem
|
3902 |
|
|
hemangioblastoma of the brainstem
|
3902 |
|
|
agenesis of the corpus callosum
|
9022 |
|
|
agenesis of the corpus callosum with peripheral neuropathy
|
902 |
|
|
agenesis of the corpus callosum with peripheral neuropathy; ACCPN
|
http://purl.obolibrary.org/obo/MONDO_0000902 |
|
|
adenoma of the liver cells
|
18902 |
|
|
amoebiasis due to Entamoeba histolytica
|
19028 |
|
|
Charcot-Marie-Tooth disease type 1 caused by mutation in NEFL
|
11902 |
|
|
Charcot-Marie-Tooth disease type 1F
|
11902 |
|
