Disease - Deafness, autosomal dominant, 39, with dentinogenesis imperfecta 1
Definition
A disorder characterized by the association of progressive sensorineural high-frequency hearing loss with dentinogenesis imperfecta.
Acronym
DFNA39/DGI1
Synonyms
DFNA39/dentinogenesis imperfecta 1 syndrome
DFNA39/DGI1 syndrome
DGI1/DFNA39 syndrome
DFNA39/DGI1 syndrome
DGI1/DFNA39 syndrome
Keywords
› Deafness
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