|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the mesomelic dysplasia, kantaputra type phenotype from the curated OMIM Gene-Disease Associations dataset.
|MMDK||Mesomelic dysplasia, Kantaputra type|