| 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.
|
vasculitides, rheumatoid
|
D056653 |
|
|
familial combined, 1 hyperlipidemia
|
C566535 |
|
|
complementation group 1 peroxisome biogenesis disorder
|
C566568 |
|
|
autosomal dominant 15 deafness
|
C566545 |
|
|
autosomal recessive 18 deafness
|
C566580 |
|
|
limb-girdle, type 1e muscular dystrophy
|
C566589 |
|
|
friedreich ataxia 2
|
C566594 |
|
|
familial restrictive, 2 cardiomyopathy
|
C566512 |
|
|
familial febrile, 2 convulsions
|
C566541 |
|
|
familial febrile, 2 seizures
|
C566541 |
|
|
hemochromatosis, type 2b
|
C566557 |
|
|
limb-girdle, type 2g muscular dystrophy
|
C566599 |
|
|
familial hemiplegic, 3 migraine
|
C566500 |
|
|
parkinson disease 3, autosomal dominant lewy body
|
C566552 |
|
|
medium chain 3-Ketoacyl-CoA thiolase deficiency
|
C566566 |
|
