|
degenerations, dry macular
|
D057092 |
|
|
amelogenesis imperfecta type IB
|
7092 |
|
|
amelogenesis imperfecta, type IB
|
7092 |
|
|
amelogenesis imperfecta, type IB; AI1B
|
http://purl.obolibrary.org/obo/MONDO_0007092 |
|
|
amelogenesis imperfecta caused by mutation in ENAM
|
7092 |
|
|
amelogenesis imperfecta caused by mutation in enam
|
7092 |
|
|
macular degeneration, dry
|
D057092 |
|
|
macular degenerations, dry
|
D057092 |
|
|
porphyrias, congenital erythropoietic
|
D017092 |
|
|
autosomal dominant hypoplastic local amelogenesis imperfecta
|
7092 |
|
|
amelogenesis imperfecta, hypoplastic local, autosomal dominant
|
7092 |
|
|
ENAM amelogenesis imperfecta
|
7092 |
|
|
enam amelogenesis imperfecta
|
7092 |
|
|
deficiency of uroporphyrinogen III synthase
|
D017092 |
|
