DSPP

dentin sialophosphoprotein
OMIM: 125485
PanelMode of inheritanceDetails
4 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
DENTINOGENESIS IMPERFECTA, SHIELDS TYPE II 125490, DEAFNESS AUTOSOMAL DOMINANT TYPE 39 WITH DENTINOGENESIS IMPERFECTA 1 605594
Green
in Hearing loss
R-numbers: R67
Signed-off version 2.5
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
hearing loss, Dentinogenesis imperfecta, Shields type II, 125490, Deafness, autosomal dominant 36, with dentinogenesis, 605594, Dentinogenesis imperfecta, Shields type III, 125500, Dentin dysplasia, type II, 125420, Dentin dysplasia, type II,1254203
R-numbers: R102
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Dentinogenesis imperfecta, Shields type II, 125490, Deafness, autosomal dominant 36, with dentinogenesis, 605594, Dentinogenesis imperfecta, Shields type III, 125500, Dentin dysplasia, type II, 125420 -3, no fractures
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Dentinogenesis imperfecta, Shields type II, 125490, Deafness, autosomal dominant 36, with dentinogenesis, 605594, Dentinogenesis imperfecta, Shields type III, 125500, Dentin dysplasia, type II, 125420 -3