SNX22, sorting nexin 22, 79856

N. diseases: 1; N. variants: 4
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C1850169
Disease: OSTEOGENESIS IMPERFECTA, TYPE IX (disorder)
OSTEOGENESIS IMPERFECTA, TYPE IX (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 2 8 0.100 None 0 4