| 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.
|
familial hyperbeta- and prebetalipoproteinemia
|
C566262 |
|
|
autosomal recessive alpha-1-Antitrypsin deficiency
|
C566273 |
|
|
familial, 1 alzheimer disease
|
C566298 |
|
|
type IV amelogenesis imperfecta
|
C566293 |
|
|
acth-independent macronodular adrenal hyperplasia
|
C565662 |
|
|
cushing syndrome, adrenal, due to aimah
|
C565662 |
|
|
acth-independent macronodular adrenocortical hyperplasia
|
C565662 |
|
|
infusion site adverse event
|
D000075662 |
|
|
injection site adverse event
|
D000075662 |
|
|
infusion site adverse reaction
|
D000075662 |
|
|
facial palsy, and retinal coloboma aortic arch interruption
|
C566271 |
|
|
malformation of arms
|
C566258 |
|
|
familial, 1 arrhythmogenic right ventricular dysplasia
|
C566254 |
|
|
rh-null disease, amorph type
|
C566210 |
|
|
psychomotor retardation, and sensorineural deafness iris dysplasia with ocular hypertelorism
|
C566234 |
|
