CCN6, cellular communication network factor 6, 8838

N. diseases: 126; N. variants: 21
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0013336
Disease: Dwarfism
Dwarfism
0.110 GeneticVariation disease BEFREE WISP3 gene mutations are associated with progressive pseudorheumatoid dysplasia (PPD, OMIM208230), an autosomal recessive genetic disease that is characterized by the swelling of multiple joints and disproportionate dwarfism. 22685593 2012
CUI: C0013336
Disease: Dwarfism
Dwarfism
0.110 Biomarker disease HPO