| 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.
|
autosomal recessive nonsyndromic deafness 105
|
14849.0 |
|
|
ventricular septal defect 3
|
13749.0 |
|
|
acquired cystic disease-associated renal cell carcinoma
|
18449.0 |
|
|
severe early-onset axonal neuropathy due to MFN2 deficiency
|
19549.0 |
|
|
hypermature cataract
|
45049.0 |
|
|
obsolete invasive pneumococcal disease, recurrent isolated
|
49.0 |
|
|
colorectal cancer, hereditary nonpolyposis, type 2
|
12249.0 |
|
|
premature aging syndrome, Okamoto type
|
11149.0 |
|
|
obsolete syringocystadenoma papilliferum
|
3449.0 |
|
|
cork-handlers' disease
|
4549.0 |
|
|
intraductal breast myoepitheliosis
|
4449.0 |
|
|
myopathy, distal, infantile-onset
|
8049.0 |
|
|
ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome
|
9149.0 |
|
|
central nervous system leiomyosarcoma
|
3349.0 |
|
|
X-linked congenital stationary night blindness
|
44749.0 |
|
