| 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.
|
lenegre-lev disease
|
C566873 |
|
|
x-linked, syndromic 13 mental retardation
|
C566875 |
|
|
protoplasmic astrocytoma (morphologic abnormality)
|
16687 |
|
|
albinoidism, oculocutaneous, autosomal dominant
|
C566872 |
|
|
SCA10 spinocerebellar ataxia 10
|
C566874 |
|
|
cardiac conduction defect, progressive
|
C566873 |
|
|
familial heart block progressive
|
C566873 |
|
|
progressive cardiac conduction defect
|
C566873 |
|
|
familial teutschlaender disease
|
C566870 |
|
|
lenegre lev disease
|
C566873 |
|
|
x-linked 79 mental retardation
|
C566876 |
|
|
oculocutaneous, autosomal dominant albinoidism
|
C566872 |
|
|
neonatal severe, due to mecp2 mutations encephalopathy
|
C566878 |
|
|
teutschlaender disease, familial
|
C566870 |
|
|
progressive familial heart block, type ia
|
C566873 |
|
