| 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.
|
hereditary spherocytosis caused by mutation in EPB42
|
12985 |
|
|
hypogonadotropic hypogonadism caused by mutation in FGF8
|
12988 |
|
|
cone-rod dystrophy caused by mutation in PROM1
|
12983 |
|
|
hereditary spherocytosis caused by mutation in SLC4A1
|
12981 |
|
|
Dioctophyme renale caused disease or disorder
|
298 |
|
|
phosphatidylcholine red cell membrane disorder
|
C535298 |
|
|
malignant germ cell neoplasm of mediastinum
|
6298 |
|
|
malignant germ cell neoplasm of the mediastinum
|
6298 |
|
|
high red cell phosphatidylcholine hemolytic anemia
|
C535298 |
|
|
leaky red cell syndrome
|
C535298 |
|
|
malignant germ cell tumor of mediastinum
|
6298 |
|
|
malignant germ cell tumor of the mediastinum
|
6298 |
|
|
mediastinal germ cell tumor, malignant
|
6298 |
|
|
aplasia of cerebellar vermis
|
7298 |
|
|
HPRT deficiency, complete
|
10298 |
|
