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MIM:250410 - RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA
Xenbase Genes: cwc27
Human Disease Resource: MIM
MONDO:0009598 - metaphyseal chondrodysplasia-retinitis pigmentosa syndrome |
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MONDO:0009598 - metaphyseal chondrodysplasia-retinitis pigmentosa syndrome |