|
2-Methyl-3-Hydroxybutyryl-CoA dehydrogenase deficiency
|
C564560 |
|
|
3-Hydroxyacyl-CoA dehydrogenase II deficiency
|
C564560 |
|
|
Hydroxyacyl-CoA dehydrogenase II deficiency
|
C564560 |
|
|
amelogenesis imperfecta caused by mutation in AMBN
|
14560 |
|
|
x-linked, syndromic 10 mental retardation
|
C564560 |
|
|
spondylometaepiphyseal dysplasia, Menger type
|
54560 |
|
|
spondyloepimetaphyseal dysplasia, anauxetic type
|
54560 |
|
|
spondylometaepiphyseal dysplasia, anauxetic type
|
54560 |
|
|
patent ductus arteriosus 1
|
24560 |
|
|
patent ductus arteriosus 1; PDA1
|
http://purl.obolibrary.org/obo/MONDO_0024560 |
|
