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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 |
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MONDO:0014700 - Au-Kline syndrome |
MONDO:0018681 - neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome |