Amelogenesis imperfecta
MONDO:0019507Amelogenesis 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.
8 clinical trials for this condition and its sub-types, 3 tagged with Amelogenesis imperfecta itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Amelogenesis imperfecta
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Hypocalcified amelogenesis imperfecta 0 trials · 3 incl. sub-types
3 sub-types
- Amelogenesis imperfecta, type 3A 3 trials
- Amelogenesis imperfecta type 3B 0 trials
- Amelogenesis imperfecta, type 3C 0 trials
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Amelogenesis imperfecta type 1G 1 trial
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Amelogenesis imperfecta type 1 0 trials
6 sub-types
- Amelogenesis imperfecta type 1A 0 trials
- Amelogenesis imperfecta type 1B 0 trials
- Amelogenesis imperfecta type 1C 0 trials
- Amelogenesis imperfecta type 1F 0 trials
- Amelogenesis imperfecta type 1H 0 trials
- Amelogenesis imperfecta, type 1J 0 trials
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Amelogenesis imperfecta type 2 0 trials
7 sub-types
- Amelogenesis imperfecta hypomaturation type 2A2 0 trials
- Amelogenesis imperfecta hypomaturation type 2A3 0 trials
- Amelogenesis imperfecta hypomaturation type 2A4 0 trials
- Amelogenesis imperfecta hypomaturation type 2A5 0 trials
- Amelogenesis imperfecta type 1E 0 trials
- Amelogenesis imperfecta type 2A1 0 trials
- Amelogenesis imperfecta, hypomaturation type, IIa6 0 trials
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Amelogenesis imperfecta, IIa 1K 0 trials