| 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.
|
paternal uniparental disomy of chromosome 1
|
16650 |
|
|
maternal uniparental disomy of chromosome 1
|
16651 |
|
|
paternal uniparental disomy of chromosome type 1
|
16650 |
|
|
maternal uniparental disomy of chromosome type 1
|
16651 |
|
|
X-linked intellectual disability-gynecomastia-obesity syndrome
|
10665 |
|
|
NAGLU Charcot-Marie-Tooth disease
|
14665 |
|
|
obsolete Refsum disease
|
21665.0 |
|
|
peroxisome biogenesis disorder, complementation group e
|
C566569 |
|
|
deafness, autosomal dominant 78
|
33665 |
|
|
familial, autosomal dominant periodic fever
|
C536657 |
|
|
familial, autosomal dominant visceral neuropathy
|
C566502 |
|
|
extrahepatic bile duct adenocarcinoma
|
2665 |
|
|
persistent muellerian duct syndrome
|
C536665 |
|
|
persistent mullerian duct syndrome
|
C536665 |
|
|
persistent müllerian duct syndrome
|
C536665 |
|
