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autosomal dominant Robinow syndrome 2

Disease Summary
Associated Targets (1)
Tchem

1


Mondo Description Any autosomal dominant Robinow syndrome in which the cause of the disease is a mutation in the DVL1 gene.
Uniprot Description A rare skeletal dysplasia syndrome characterized by dysmorphic features resembling a fetal face, mesomelic limb shortening, hypoplastic external genitalia in males, costovertebral segmentation defects, and renal anomalies.
Mondo Term and Equivalent IDs
MONDO:0014591:  autosomal dominant Robinow syndrome 2
UMLS:C4225363: