syndromic disease cleidorhizomelic syndrome https://github.com/monarch-initiative/mondo/issues/6751 https://github.com/monarch-initiative/mondo/issues/6877 https://rarediseases.info.nih.gov/diseases/5532/cleidorhizomelic-syndrome https://www.malacards.org/card/cleidorhizomelic_syndrome OMIM:119650 brachydactyly, enlarged diaphysis, rhizomelic micromelia, short stature and abnormal clavicle UMLS:C1861515 cleidorhizomelic syndrome Cleidorhizomelic syndrome is a rhizo-mesomelic dysplasia characterized by rhizomelic short stature/dwarfism in combination with lateral clavicular defects. Additional manifestations include brachydactyly with bilateral clinodactyly and hypoplastic middle phalanx of the fifth digit. X-ray demonstrated an apparent Y-shaped or bifid distal clavicle. Cleidorhizomelic syndrome has been reported in one family (mother and son) and is suspected to be transmitted in an autosomal dominant manner. There have been no further descriptions in the literature since 1988. SCTID:719471002 Wallis-Zieff-Goldblatt syndrome Orphanet:1453 MESH:C536428 Wallis Zieff Goldblatt syndrome cleido rhizomelic syndrome MONDO:0007341 MEDGEN:350042 GARD:0005532 rhizomelic shortness with clavicular defect skeletal dysplasia