| manager |
|
| language |
- |
| license |
- |
| created at |
2021-12-20 02:12:37 UTC |
| updated at |
2021-12-22 07:05:13 UTC |
|
MONDO_prefferred_names from the Bioportal site.
|
24,286 entries
|
There is 0 pattern entry.
|
congenital stationary night blindness 1G
|
14614.0 |
|
|
dextrocardia with unusual facies and microphthalmia
|
9098.0 |
|
|
ocular toxoplasmosis
|
5879.0 |
|
|
candidiasis, familial, 4
|
13140.0 |
|
|
skin appendage disease
|
24481.0 |
|
|
corticosteroid-induced osteoporosis
|
24651.0 |
|
|
oculocutaneous albinism type 7
|
14070.0 |
|
|
periventricular nodular heterotopia 6
|
14240.0 |
|
|
steatitis
|
6979.0 |
|
|
Wolman disease with hypolipoproteinemia and acanthocytosis
|
10205.0 |
|
|
Smith-Lemli-Opitz syndrome
|
10035.0 |
|
|
hereditary lymphedema
|
19313.0 |
|
|
intestinal cancer
|
5814.0 |
|
|
obesity-hypoventilation syndrome
|
9763.0 |
|
|
obsolete POEMS syndrome
|
6914.0 |
|
