|
enamel hypoplasia, hereditary localized
|
7092 |
|
|
amelogenesis imperfecta, hypoplastic local, autosomal dominant
|
7092 |
|
|
ENAM amelogenesis imperfecta
|
7092 |
|
|
enam amelogenesis imperfecta
|
7092 |
|
|
amelogenesis imperfecta type IB
|
7092 |
|
|
degeneration, dry macular
|
D057092 |
|
|
degenerations, dry macular
|
D057092 |
|
|
erythropoietic, congenital porphyria
|
D017092 |
|
|
congenital erythropoietic porphyrias
|
D017092 |
|
|
amelogenesis imperfecta, type IB
|
7092 |
|
|
amelogenesis imperfecta, type IB; AI1B
|
http://purl.obolibrary.org/obo/MONDO_0007092 |
|
|
amelogenesis imperfecta type 1B
|
7092 |
|
|
amelogenesis imperfecta, type 1B
|
7092 |
|
|
deficiency of uroporphyrinogen III synthase
|
D017092 |
|
