langer mesomelic dysplasia Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Langer mesomelic dysplasia (LMD) is characterized by severe disproportionate short stature with mesomelic and rhizomelic shortening of the upper and lower limbs. (Orphanet Rare Disease Ontology, Orphanet_2632)
External Link http://www.omim.org/entry/249700
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Genes

1 genes associated with the langer mesomelic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SHOX short stature homeobox