|
ruptures, post-infarction cardiac
|
D006342 |
|
|
post infarction cardiac rupture
|
D006342 |
|
|
Meier-Gorlin syndrome caused by mutation in ORC4
|
13428 |
|
|
retinitis pigmentosa caused by mutation in PDE6B
|
13429 |
|
|
retinitis pigmentosa caused by mutation in RPE65
|
13425 |
|
|
O'nyong-nyong virus caused disease or disorder
|
342 |
|
|
adenoma, clear cell, benign
|
3426 |
|
|
syndrome, treacher collins
|
D008342 |
|
|
syndrome, treacher collins-franceschetti
|
D008342 |
|
|
syndromes, treacher collins-franceschetti
|
D008342 |
|
|
type II complement component 8 deficiency
|
13421 |
|
|
type I complement component 8 deficiency
|
13422 |
|
|
type i complement component 8 deficiency
|
http://purl.obolibrary.org/obo/MONDO_0013422 |
|
