| 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.
|
invasive hydatidiform mole
|
20549.0 |
|
|
non-neoplastic nevus
|
22749.0 |
|
|
transcobalamin II deficiency
|
10149.0 |
|
|
defective apolipoprotein b-100
|
22949.0 |
|
|
N-acetylaspartate deficiency
|
13549.0 |
|
|
intellectual disability, autosomal recessive 50
|
14649.0 |
|
|
Sotos syndrome
|
19349.0 |
|
|
finger hyperphalangy - toe anomalies - severe pectus excavatum syndrome
|
18249.0 |
|
|
osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures
|
8149.0 |
|
|
osteoma of cranial vault, familial
|
11349.0 |
|
|
spinocerebellar ataxia type 23
|
12449.0 |
|
|
drug- or toxin-induced pulmonary arterial hypertension
|
17149.0 |
|
|
congenital myopathy, Paradas type
|
16049.0 |
|
|
obsolete X-linked B cell surface antigen, mouse, homolog-like 1
|
10249.0 |
|
|
hypotrichosis 9
|
13649.0 |
|