DSPP, dentin sialophosphoprotein, 1834

N. diseases: 114; N. variants: 13
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0399380
Disease: Dentin dyspalsia, Shields type 2
Dentin dyspalsia, Shields type 2 		0.770 Biomarker disease CTD_human
CUI: C0399380
Disease: Dentin dyspalsia, Shields type 2
Dentin dyspalsia, Shields type 2 		0.770 CausalMutation disease CLINVAR
CUI: C0399380
Disease: Dentin dyspalsia, Shields type 2
Dentin dyspalsia, Shields type 2 		0.770 GermlineCausalMutation disease ORPHANET
CUI: C0399380
Disease: Dentin dyspalsia, Shields type 2
Dentin dyspalsia, Shields type 2 		0.770 Biomarker disease GENOMICS_ENGLAND
CUI: C2973527
Disease: Dentinogenesis imperfecta without osteogenesis imperfecta
Dentinogenesis imperfecta without osteogenesis imperfecta 		0.770 Biomarker disease CTD_human
CUI: C2973527
Disease: Dentinogenesis imperfecta without osteogenesis imperfecta
Dentinogenesis imperfecta without osteogenesis imperfecta 		0.770 CausalMutation disease CLINVAR
CUI: C2973527
Disease: Dentinogenesis imperfecta without osteogenesis imperfecta
Dentinogenesis imperfecta without osteogenesis imperfecta 		0.770 Biomarker disease GENOMICS_ENGLAND
CUI: C2973527
Disease: Dentinogenesis imperfecta without osteogenesis imperfecta
Dentinogenesis imperfecta without osteogenesis imperfecta 		0.770 GermlineCausalMutation disease ORPHANET
CUI: C0399378
Disease: Dentinogenesis imperfecta - Shield's type III (disorder)
Dentinogenesis imperfecta - Shield's type III (disorder) 		0.710 CausalMutation disease CLINVAR
CUI: C0399378
Disease: Dentinogenesis imperfecta - Shield's type III (disorder)
Dentinogenesis imperfecta - Shield's type III (disorder) 		0.710 Biomarker disease CTD_human
CUI: C0399378
Disease: Dentinogenesis imperfecta - Shield's type III (disorder)
Dentinogenesis imperfecta - Shield's type III (disorder) 		0.710 Biomarker disease GENOMICS_ENGLAND
CUI: C0399378
Disease: Dentinogenesis imperfecta - Shield's type III (disorder)
Dentinogenesis imperfecta - Shield's type III (disorder) 		0.710 GermlineCausalMutation disease ORPHANET
CUI: C0011436
Disease: Dentinogenesis Imperfecta
Dentinogenesis Imperfecta 		0.700 Biomarker disease HPO
CUI: C0011436
Disease: Dentinogenesis Imperfecta
Dentinogenesis Imperfecta 		0.700 Biomarker disease CTD_human
CUI: C1854146
Disease: Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1
Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 		0.700 Biomarker disease CTD_human
CUI: C1854146
Disease: Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1
Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C1854146
Disease: Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1
Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 		0.700 GeneticVariation disease CLINVAR
CUI: C4049050
Disease: Opalescent dentin
Opalescent dentin 		0.520 Biomarker disease GENOMICS_ENGLAND
CUI: C4049050
Disease: Opalescent dentin
Opalescent dentin 		0.520 Biomarker disease CTD_human
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.400 GeneticVariation phenotype CLINVAR
CUI: C0399379
Disease: Dentin dysplasia, type 1
Dentin dysplasia, type 1 		0.310 GermlineCausalMutation disease ORPHANET
CUI: C0205730
Disease: Hereditary Opalescent Dentin (disorder)
Hereditary Opalescent Dentin (disorder) 		0.300 Biomarker disease CTD_human
CUI: C0018780
Disease: Hearing Loss, High-Frequency
Hearing Loss, High-Frequency 		0.100 Biomarker disease HPO
CUI: C0040264
Disease: Tinnitus
Tinnitus 		0.100 Biomarker phenotype HPO
CUI: C0266060
Disease: Anterior open bite
Anterior open bite 		0.100 Biomarker disease HPO