Schmid metaphyseal chondrodysplasia

MONDO:0007983

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.

Also known as: MCDS, Metaphyseal Chondrodysplasia, Schmid Type, metaphyseal chondrodysplasia Schmid type, metaphyseal chondrodysplasia, Schmid type, spondylometaphyseal dysplasia, Japanese type

0 clinical trials for this condition and its sub-types, 0 tagged with Schmid metaphyseal chondrodysplasia itself.

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↑ Syndromic disease (7133) ↑ Osteochondrodysplasia (380)

Including sub-types (0) Tagged with Schmid metaphyseal chondrodysplasia (0)

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