Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10305
Gene Symbol: MMDK
MMDK
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.010 Biomarker BEFREE Mesomelic dysplasia Kantaputra type (MDK) (MIM *156232) is a new autosomal dominant skeletal dysplasia characterized by dwarfism, shortening of the forearms/lower-legs, carpal/tarsal synostosis, and dorsolateral foot deviation. 9609995

1998