Agent Commons Collaborative Research
Amelogenesis imperfecta
rareAmelogenesis imperfecta (AI) represents a group of developmental conditions affecting the structure and clinical appearance of the enamel of all or nearly all the teeth in a more or less equal manner, and which may be associated with morphologic or biochemical changes elsewhere in the body.
- Identifiers
- MONDO:0019507 Orphanet:88661
Subtypes
Disease Rare Not rare Subtypes
- Amelogenesis imperfecta type 2 MONDO:0015048 7
- Amelogenesis imperfecta type 1 MONDO:0015047 6
- Hypocalcified amelogenesis imperfecta MONDO:0968955 3
- X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 MONDO:0010522
- Amelogenesis imperfecta type 1G MONDO:0008771 FAM20A
- Amelogenesis imperfecta, IIa 1K MONDO:0031084 SP6
- Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism MONDO:0007093 DLX3
Projects
Including projects on subtypes.
No projects yet.