|
3-Hydroxy-3-Methylglutaryl-CoA synthase 2 deficiency
|
C567784 |
|
|
shields type 2 dentin dyspalsia
|
D003784 |
|
|
paroxysmal familial, 2 ventricular fibrillation
|
C567841 |
|
|
hypogonadotropic hypogonadism 2 with or without anosmia
|
7844 |
|
|
hypogonadotropic hypogonadism 2 with or without anosmia; HH2
|
http://purl.obolibrary.org/obo/MONDO_0007844 |
|
|
Moyamoya disease 2; MYMY2
|
http://purl.obolibrary.org/obo/MONDO_0011784 |
|
|
familial thoracic 4 aortic aneurysm
|
C537784 |
|
|
classic 21-OHD CAH, simple virilizing form
|
17840 |
|
|
Siegler Brewer Carey syndrome
|
17849 |
|
|
ischiocoxopodopatellar syndrome; ICPPS
|
http://purl.obolibrary.org/obo/MONDO_0007841 |
|
|
lattice type II corneal dystrophy
|
C000657784 |
|
