| 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.
|
T-B+ severe combined immunodeficiency due to gamma chain deficiency
|
10315 |
|
|
T-B+ severe combined immunodeficiency, X-linked
|
10315 |
|
|
fibula aplasia complex brachydactyly
|
23155 |
|
|
neonatal ovarian cyst
|
43154 |
|
|
familial multilocular cystic disease of the jaws
|
7315 |
|
|
factor XII deficiency disease
|
9315 |
|
|
chromosome 10q26 deletion syndrome
|
12315 |
|
|
distal 10q deletion syndrome
|
12315 |
|
|
iduronate 2-sulfatase deficiency type A
|
16315 |
|
|
chromosome 10q deletion
|
12315 |
|
|
craniosynostosis 7, digenic
|
44315 |
|
|
Hageman Factor deficiency
|
9315 |
|
|
factor 12 deficiency
|
9315 |
|
|
factor XII deficiency
|
9315 |
|
|
inflammatory bowel disease type 28
|
13153 |
|
