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MIM:614195 - CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME; CAASDS
Xenbase Genes: vsx1
Human Disease Resource: MIM
MONDO:0013618 - craniofacial anomalies and anterior segment dysgenesis syndrome |
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MONDO:0013618 - craniofacial anomalies and anterior segment dysgenesis syndrome |