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MIM:614815 - JOUBERT SYNDROME 18; JBTS18
Xenbase Genes: tctn3
Human Disease Resource: MIM
| MONDO:0010176 - orofaciodigital syndrome type 6 |
| MONDO:0013896 - Joubert syndrome 18 |
|
| MONDO:0010176 - orofaciodigital syndrome type 6 |
| MONDO:0013896 - Joubert syndrome 18 |