Mondo Description Autosomal recessive form of omodysplasia.
Uniprot Description A rare autosomal recessive skeletal dysplasia characterized by facial dysmorphism and severe congenital micromelia with shortening and distal tapering of the humeri and femora, to give a club-like appearance. Typical facial features include a prominent forehead, frontal bossing, short nose with a depressed broad bridge, short columella, anteverted nostrils, long philtrum, and small chin.
Mondo Term and Equivalent IDs
MONDO:0009779: autosomal recessive omodysplasia