|
primary ciliary dyskinesia 30
|
14465 |
|
|
primary ciliary dyskinesia 30 without situs inversus
|
14465 |
|
|
primary ciliary dyskinesia 32
|
14657 |
|
|
primary ciliary dyskinesia 32 without situs inversus
|
14657 |
|
|
primary ciliary dyskinesia caused by mutation in CCDC151
|
14465 |
|
|
MME-related autosomal dominant CMT2
|
44657 |
|
|
MME-related autosomal dominant Charcot Marie Tooth disease type 2
|
44657 |
|
|
primary ciliary dyskinesia caused by mutation in RSPH3
|
14657 |
|
|
primary ciliary dyskinesia type 30
|
14465 |
|
|
MME-related autosomal dominant hereditary motor and sensory neuropathy type 2
|
44657 |
|
|
hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
|
12465 |
|
|
immune defect due to inosine phosphorylase deficiency
|
C565465 |
|
|
primary ciliary dyskinesia type 32
|
14657 |
|
|
POLR1A acrofacial dysostosis
|
14651 |
|
|
arthrogryposis, ectodermal dysplasia, cleft lip-palate, and developmental delay
|
C535465 |
|
