mesomelic dysplasia, kantaputra type Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Mesomelic dysplasia Kantaputra type (MDK) is a rare skeletal disease characterized by symmetric shortening of the middle segments of limbs and short stature. (Orphanet Rare Disease Ontology, Orphanet_1836)
External Link http://www.omim.org/entry/156232
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Genes

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

Symbol Name
MMDK Mesomelic dysplasia, Kantaputra type