|
MIM:616580 - AU-KLINE SYNDROME; AUKS
Xenbase Genes: hnrnpk
Human Disease Resource: MIM
| MONDO:0014700 - Au-Kline syndrome |
| MONDO:0018681 - neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome |
|
| MONDO:0014700 - Au-Kline syndrome |
| MONDO:0018681 - neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome |