| 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.
|
total premature chromatid separation trait
|
8304 |
|
|
ring 18 chromosome syndrome
|
C538304 |
|
|
autosomal recessive complex spastic paraplegia caused by mutation in ARL6IP1
|
14304 |
|
|
oxidase deficiencies, cytochrome
|
D030401 |
|
|
oxidase deficiency, cytochrome
|
D030401 |
|
|
Cytochrome-c oxidase deficiencies
|
D030401 |
|
|
complex IV deficiencies
|
D030401 |
|
|
cytochrome oxidase deficiencies
|
D030401 |
|
|
enolase 3 deficiency
|
13046 |
|
|
muscle enolase deficiency
|
13046 |
|
|
muscular enolase deficiency
|
13046 |
|
|
LDH-M subunit deficiency
|
13047 |
|
|
Protein S deficiency
|
2304 |
|
|
protein S deficiency
|
2304 |
|
|
Cytochrome-c oxidase deficiency
|
D030401 |
|
