|
primary ciliary dyskinesia caused by mutation in RSPH3
|
14657 |
|
|
primary ciliary dyskinesia type 32
|
14657 |
|
|
POLR1A acrofacial dysostosis
|
14651 |
|
|
RNASEH1 progressive external ophthalmoplegia with mitochondrial DNA deletions
|
14656 |
|
|
infantile liver failure caused by mutation in NBAS
|
14659 |
|
|
infantile liver failure syndrome 2
|
14659 |
|
|
infantile liver failure syndrome 2; ILFS2
|
http://purl.obolibrary.org/obo/MONDO_0014659 |
|
|
infantile liver failure syndrome type 2
|
14659 |
|
|
NBAS infantile liver failure
|
14659 |
|
|
familial temporal lobe epilepsy 8
|
14650 |
|
|
familial temporal lobe epilepsy type 8
|
14650 |
|
|
ciliary dyskinesia, primary, 32
|
14657 |
|
|
Ullrich congenital muscular dystrophy 2
|
14654 |
|
|
Ullrich congenital muscular dystrophy 2; UCMD2
|
http://purl.obolibrary.org/obo/MONDO_0014654 |
|
