Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:250410 - RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA


Xenbase Genes: cwc27

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009598 - metaphyseal chondrodysplasia-retinitis pigmentosa syndrome