DSPP, dentin sialophosphoprotein, 1834

N. diseases: 114; N. variants: 13
Disease: Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 ×
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: C1854146
Disease: Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1
Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 1 3 0.700 None 1.000 5 3 1997 2017