|
Ullrich congenital muscular dystrophy type 2
|
14654 |
|
|
progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RNASEH1
|
14656 |
|
|
benign neoplasm of the appendix
|
21465 |
|
|
benign tumor of the appendix
|
21465 |
|
|
benign neoplasm of appendix
|
21465 |
|
|
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2
|
14656 |
|
|
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2; PEOB2
|
http://purl.obolibrary.org/obo/MONDO_0014656 |
|
|
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 2
|
14656 |
|
|
progressive external ophthalmoplegia, autosomal recessive 2
|
14656 |
|
|
ZNF408 retinitis pigmentosa
|
14653 |
|
|
ZNF408 exudative vitreoretinopathy
|
14652 |
|
|
ciliary dyskinesia, primary, 32
|
14657 |
|
|
ciliary dyskinesia, primary, 32, without situs inversus
|
14657 |
|
|
ciliary dyskinesia, primary, 32; CILD32
|
http://purl.obolibrary.org/obo/MONDO_0014657 |
|
