Amelogenesis imperfecta type 1B

Definition

Any amelogenesis imperfecta in which the cause of the disease is a mutation in the ENAM gene.

Also known as AI1B, amelogenesis imperfecta caused by mutation in ENAM, ENAM amelogenesis imperfecta, hereditary localised enamel hypoplasia — per MONDO

Also identified as

• DOID 0110052 per MONDO
• ICD9 520.5 per MONDO
• MESH C562879 per MONDO
• OMIM 104500 per MONDO
• SCTID 234961008 per MONDO
• UMLS C0399368 per MONDO