| 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.
|
mecp2-related severe neonatal encephalopathy
|
C566878 |
|
|
encephalopathy, neonatal severe, due to mecp2 mutations
|
C566878 |
|
|
burning mouth syndrome
|
6687 |
|
|
hyperphosphatemic, familial tumoral calcinosis
|
C566870 |
|
|
x-linked, with spasticity mental retardation
|
C566877 |
|
|
weaver smith syndrome
|
C536687 |
|
|
progressive familial, type 1 heart block
|
C566873 |
|
|
mental retardation, x-linked 79
|
C566876 |
|
|
mental retardation, x-linked, syndromic 13
|
C566875 |
|
|
mental retardation, x-linked, with spasticity
|
C566877 |
|
|
x-linked 79 mental retardation
|
C566876 |
|
|
tumoral calcinosis, primary hyperphosphatemic
|
C566870 |
|
|
type ia progressive familial heart block
|
C566873 |
|
|
heart block, progressive familial, type i
|
C566873 |
|
|
heart block progressive, familial
|
C566873 |
|
