(Q55783418)
English
deafness, autosomal dominant 39, with dentinogenesis imperfecta 1
human disease
- Dfna39/Dentinogenesis Imperfecta 1 Syndrome
- Dfna39/Dgi1 Syndrome
- Deafness, Autosomal Dominant 39, With Dentinogenesis Imperfecta type 1
- DEAFNESS, AUTOSOMAL DOMINANT 39, WITH DENTINOGENESIS IMPERFECTA 1
- Dgi1/Dfna39 Syndrome
Statements
2 references
Identifiers
1 reference
1 reference
1 reference