| 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.
|
neuronal intestinal dysplasia
|
858.0 |
|
|
immunodeficiency 75
|
30858.0 |
|
|
mitochondrial complex 5 (ATP synthase) deficiency nuclear type 5
|
20858.0 |
|
|
pontine tegmental cap dysplasia
|
13858.0 |
|
|
intellectual disability, autosomal dominant 43
|
14858.0 |
|
|
Graham Little-Piccardi-Lassueur syndrome
|
18858.0 |
|
|
occlusion of gallbladder
|
4858.0 |
|
|
acute erythroid leukemia
|
17858.0 |
|
|
ovary rhabdomyosarcoma
|
2858.0 |
|
|
anterior optic tract meningioma
|
3858.0 |
|
|
continuous spike-wave during slow sleep syndrome
|
22858.0 |
|
|
blepharophimosis-epicanthus inversus-ptosis due to a point mutation syndrome
|
16858.0 |
|
|
inherited fatty acid metabolism disorder
|
37858.0 |
|
|
Tietze syndrome
|
1858.0 |
|
|
primary CD59 deficiency
|
12858.0 |
|
