|
high serum cholesterol, familial
|
C538646 |
|
|
type 2 a hyperlipoproteinemia
|
C538646 |
|
|
infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome
|
33864 |
|
|
hyperlipoproteinemia, type 2 a
|
C538646 |
|
|
Cornelia DE Lange syndrome 4
|
13864 |
|
|
Cornelia de Lange syndrome 4
|
13864 |
|
|
Cornelia DE Lange syndrome 4; CDLS4
|
http://purl.obolibrary.org/obo/MONDO_0013864 |
|
|
Cornelia de Lange syndrome caused by mutation in RAD21
|
13864 |
|
|
Cornelia De Lange syndrome type 4
|
13864 |
|
|
familial high serum cholesterol
|
C538646 |
|
|
Limb-girdle muscular dystrophy autosomal recessive
|
C538640 |
|
