|
endocardium neoplasm (disease)
|
21378 |
|
|
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 |
|
|
cone-ROD dystrophy 16; CORD16
|
http://purl.obolibrary.org/obo/MONDO_0013786 |
|
|
retinitis pigmentosa 63; RP63
|
http://purl.obolibrary.org/obo/MONDO_0013780 |
|
|
psychomotor retardation, epilepsy, and craniofacial dysmorphism
|
13787 |
|
|
meconium ileus 1N cystic fibrosis, susceptibility to
|
http://purl.obolibrary.org/obo/MONDO_0011378 |
|
