DISEASES

Disease-gene associations mined from literature

JensenLab

Human genes for dentinogenesis imperfecta

Dentinogenesis imperfecta [DOID:4154]

A tooth disease characterized by discolored, opalescent teeth that has_material_basis_in mutation in the DSPP gene on chromosome 4q22.

Synonyms:  dentinogenesis imperfecta,  DOID:4154,  dentinogenesis imperfectas

Linkouts:  OMIM #1 #2