Autosomal recessive Robinow syndrome

MONDO:0009999

Autosomal recessive Robinow syndrome (RRS) is the less common type of Robinow syndrome (RS) characterized by short-limb dwarfism, costovertebral segmentation defects and abnormalities of the head, face and external genitalia.

Also known as: COVESDEM syndrome, RRS, Robinow syndrome, autosomal recessive, costovertebral segmentation defect-mesomelia syndrome, Covesdem syndrome, Covesdem syndrome, formerly, Robinow syndrome, autosomal recessive, with Brachy-syn-polydactyly, Robinow syndrome, autosomal recessive, with aplasia/hypoplasia of phalanges and metacarpals/metatarsals

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

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↑ Autosomal recessive disease (999) ↑ Robinow syndrome (0)

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

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