toIPA
Home
Blog
Category
Smith-mccort dysplasia
osteochondrodysplasia characterized by short limbs and a short trunk with a barrel-shaped chest and has material basis in homozygous or compound heterozygous mutation in the DYM gene on chromosome 18q
Pronunciation
/smɪθ - məˈkɔrt dɪsˈpleɪʒiə/
Categories
disease
Dyggve–Melchior–Clausen syndrome
spondyloepimetaphyseal dysplasia
rare disease