D000567Level 6
Amelogenesis Imperfecta
**Definition:** A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION.
**Tree numbers:** - C07.650.800.295.250 - C07.793.700.295.250 - C16.131.850.800.295.250
**Synonyms:** - Congenital Enamel Hypoplasia
GET
/api/v1/systems/mesh/nodes/D000567Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.