|
primary ciliary dyskinesia type 11
|
12978 |
|
|
deafness, autosomal dominant 3B; DFNA3B
|
http://purl.obolibrary.org/obo/MONDO_0012975 |
|
|
primary ciliary dyskinesia type 12
|
12979 |
|
|
cleidocranial digital dysostoses
|
D002973 |
|
|
deafness, autosomal dominant 59
|
12974 |
|
|
deafness, autosomal dominant 59; DFNA59
|
http://purl.obolibrary.org/obo/MONDO_0012974 |
|
|
cleidocranial digital dysostosis
|
D002973 |
|
|
diaphragmatic hernia exomphalos corpus callosum agenesis
|
22977 |
|
|
limb-girdle muscular dystrophy type 1H
|
13297 |
|
|
Herpesviridae infectious embryofetopathy
|
42971 |
|
|
short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies
|
100297 |
|
|
trichoepithelioma, multiple familial, 1
|
42977 |
|
|
febrile seizures, familial, 10
|
12972 |
|
|
febrile seizures, familial, 10; FEB10
|
http://purl.obolibrary.org/obo/MONDO_0012972 |
|
|
short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1
|
100297 |
|
