SLC20A1, solute carrier family 20 member 1, 6574

N. diseases: 87; N. variants: 1
Disease: Achondroplasia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		0.010 GeneticVariation disease BEFREE GH-1 and Pit-1 gene analyses are crucial, when genetic abnormalities other than achondroplasia are suspected. 16618986 2006