| 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.
|
multiple mitochondrial dysfunctions syndrome 2; MMDS2
|
http://purl.obolibrary.org/obo/MONDO_0013675 |
|
|
multiple mitochondrial dysfunctions syndrome type 2
|
13675 |
|
|
facial nevi and mental changes arteriovenous aneurysm of mid-brain and retina
|
C536752 |
|
|
mental retardation X-linked severe gustavson type
|
C536759 |
|
|
BOLA3 fatal multiple mitochondrial dysfunctions syndrome
|
13675 |
|
|
posterolateral myocardial infarction
|
3675 |
|
|
deletion xp22 pter
|
C536754 |
|
|
fatal multiple mitochondrial dysfunctions syndrome caused by mutation in BOLA3
|
13675 |
|
|
x chromosome, monosomy xp22 pter
|
C536754 |
|
|
x chromosome, monosomy xq28
|
C536755 |
|
|
monosomy xp22 pter
|
C536754 |
|
|
monosomy xp22 pter x chromosome
|
C536754 |
|
|
deafness, and seizures mental retardation with optic atrophy
|
C536759 |
|
|
wyburn Mason's syndrome
|
C536752 |
|
|
X-linked mental retardation gustavson type
|
C536759 |
|
