Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome (CAASDS)

Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome(来自ICD-11)

别称:

Caasds

Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome (caasds

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome, is also known as caasds. An important gene associated with Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome is VSX1 (Visual System Homeobox 1). Affiliated tissues include pituitary and endothelial, and related phenotypes are anterior synechiae of the anterior chamber and abnormal pinna morphology

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