has characteristic has characteristic has material basis in germline mutation in ROR2 Autosomal recessive inheritance autosomal recessive disease autosomal recessive Robinow syndrome https://github.com/monarch-initiative/mondo/issues/4948 https://www.malacards.org/card/autosomal_recessive_robinow_syndrome https://www.malacards.org/card/robinow_syndrome_autosomal_recessive_1 costovertebral segmentation defect-mesomelia syndrome icd11.foundation:793292660 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. MONDO:0009999 Orphanet:1507 DOID:0060764 Robinow syndrome, autosomal recessive GARD:0016568 COVESDEM syndrome costovertebral segmentation defect with mesomelia RRS Covesdem syndrome OMIM:268310 MEDGEN:1770070 MESH:C535863 UMLS:C5399974 Robinow syndrome