Autosomal dominant Robinow syndrome

rare

Autosomal dominant Robinow syndrome (DRS) is the more common type of Robinow syndrome (RS) characterized by mild to moderate limb shortening and abnormalities of the head, face and external genitalia.

Identifiers: MONDO:0008389 Orphanet:3107
Part of: Robinow syndrome Autosomal dominant disease
Also known as: Robinow syndrome, autosomal dominant · Robinow syndrome, autosomal dominant type

Subtypes

All diseases Rare only

Disease	ID	Genes
Autosomal dominant Robinow syndrome 1	MONDO:0024455	WNT5A
Autosomal dominant Robinow syndrome 2	MONDO:0014591	DVL1
Autosomal dominant Robinow syndrome 3	MONDO:0014819	DVL3

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