Autosomal recessive Robinow syndrome (Q101943)
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Autosomal recessive Robinow syndrome (RRS) is the less common and the more severe type of Robinow syndrome (RS) characterised by short-limb dwarfism, costovertebral segmentation defects and abnormalities of the head, face and external genitalia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_793292660 |
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| English | Autosomal recessive Robinow syndrome |
Autosomal recessive Robinow syndrome (RRS) is the less common and the more severe type of Robinow syndrome (RS) characterised by short-limb dwarfism, costovertebral segmentation defects and abnormalities of the head, face and external genitalia. |
Statements
CID11:ID_793292660
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dki-india-ID_793292660
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Concluído
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15 August 2026
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