Robinow syndrome

MONDO:0019978

Robinow syndrome (RS) is a rare genetic syndrome characterized by limb shortening and abnormalities of the head, face and external genitalia.

Also known as: Robinow dwarfism, Robinow-Silverman-Smith syndrome, acral dysostosis with facial and genital abnormalities, fetal face syndrome, foetal face syndrome, mesomelic dwarfism-small genitalia syndrome, Covesdem syndrome (formerly), costovertebral segmentation defect with mesomelia (formerly)

0 clinical trials for this condition and its sub-types, 0 tagged with Robinow syndrome itself.

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Where it sits in the disease tree

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Part of

↑ Syndromic disease (7133) ↑ Skeletal dysplasia (660) ↑ Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome (90)

Sub-types of Robinow syndrome

Autosomal dominant Robinow syndrome 0 trials
3 sub-types
- Autosomal dominant Robinow syndrome 1 0 trials
- Autosomal dominant Robinow syndrome 2 0 trials
- Autosomal dominant Robinow syndrome 3 0 trials
Autosomal recessive Robinow syndrome 0 trials
Robinow syndrome, autosomal recessive 2 0 trials

Including sub-types (0) Tagged with Robinow syndrome (0)

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