|
orofacial cleft 10; OFC10
|
http://purl.obolibrary.org/obo/MONDO_0013378 |
|
|
cone-ROD dystrophy 16; CORD16
|
http://purl.obolibrary.org/obo/MONDO_0013786 |
|
|
meconium ileus 1N cystic fibrosis, susceptibility to
|
http://purl.obolibrary.org/obo/MONDO_0011378 |
|
|
pseudohypoaldosteronism type 2 caused by mutation in CUL3
|
13782 |
|
|
pseudohypoaldosteronism type 2 caused by mutation in Cul3
|
13782 |
|
|
pseudohypoaldosteronism type 2 caused by mutation in KLHL3
|
13781 |
|
|
shields type 2 dentin dyspalsia
|
D003784 |
|
|
congenital motor, 2 nystagmus
|
C537854 |
|
|
pseudohypoaldosteronism type 2D
|
13781 |
|
|
pseudohypoaldosteronism, type 2D
|
13781 |
|
|
pseudohypoaldosteronism type 2E
|
13782 |
|
|
pseudohypoaldosteronism, type 2E
|
13782 |
|
|
fibromatosis, gingival, 3
|
12378 |
|
