| Label | Id | |
|---|---|---|
| COXPD9 | 13811 | |
| herrmann syndrome | C538113 | |
| X-linked laterality | C538116 | |
| visceral heterotaxia | C538116 | |
| capdepont teeth | D003811 | |
| dentin, opalescent | D003811 | |
| teeth, capdepont | D003811 | |
| heterotaxy, visceral, 1, x-linked | C538116 | |
| shields type 2 dentinogenesis imperfecta | D003811 | |
| human herpesvirus 6 encephalitis | C538117 | |
| shields type II dentinogenesis imperfecta | D003811 | |
| visceral, 5, autosomal heterotaxy | C538116 | |
| situs inversus, complex cardiac defects, and splenic defects, X-linked | C538116 | |
| diabetes mellitus, deafness, nephropathy, and cerebral dysfunction photomyoclonus | C538113 | |
| complex cardiac defects, and splenic defects, X-linked situs inversus | C538116 |