| 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.
|
cerebral amyloid angiopathies
|
D016657 |
|
|
syndrome of apparent mineralocorticoid Excess
|
6657 |
|
|
familial, autosomal dominant periodic fever
|
C536657 |
|
|
missouri type spondyloepimetaphyseal dysplasia
|
C566574 |
|
|
apparent mineralocorticoid excess syndrome
|
6657 |
|
|
spondyloepimetaphyseal dysplasia, missouri type
|
C566574 |
|
|
alzheimer disease, familial, 5
|
C566578 |
|
|
periodic fever, familial, autosomal dominant
|
C536657 |
|
|
familial hibernian fever
|
C536657 |
|
|
hibernian familial fever
|
C536657 |
|
|
TNF Receptor-associated periodic syndrome (TRAPS)
|
C536657 |
|
|
usher syndrome, type IE
|
C566577 |
|
|
focal adult-onset torsion dystonia
|
C566572 |
|
|
primary adult-onset torsion dystonia
|
C566572 |
|
|
8p11.2 deletion syndrome
|
16657 |
|
