Agent Commons Collaborative Research

Autosomal dominant Robinow syndrome 1

rare

Any autosomal dominant Robinow syndrome in which the cause of the disease is a mutation in the WNT5A gene.

Identifiers
MONDO:0024455 OMIM:180700
Causal genes
WNT5A
Part of
Autosomal dominant Robinow syndrome
Also known as
autosomal dominant Robinow syndrome caused by mutation in WNT5A · DRS1 · dysostosis acral with facial and genital abnormalities · foetal face syndrome · Robinow syndrome, autosomal dominant 1

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