amelogenesis imperfecta
MONDO:0019507- MONDO:
- MONDO:0019507
- Orphanet:
- 88661 ↗
Rare disease41 associated genes
Description
Amelogenesis 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.
Associated genes
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