A rare skeletal disorder caused by a variation in COL10A1 gene and is characterized by moderately short stature with short limbs, coxa vara, bowlegs and an abnormal gait. The disease is Schmid metaphyseal chondrodysplasia (Monarch Disease Ontology entry MONDO_0007983). Also known as: Japanese type spondylometaphyseal dysplasia, MCDS, Metaphyseal Chondrodysplasia, Schmid Type, Schmid type metaphyseal dysplasia, metaphyseal chondrodysplasia Schmid type, metaphyseal chondrodysplasia, Schmid type, spondylometaphyseal dysplasia, Japanese type.