Amelogenesis imperfecta

Orpha code: 88661OMIM code: 617217

Definition

A rare genetic odontal or periodontal disorder that 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.

Disease data
Classification

Disease

ORPHA code
88661
OMIM code
617217
ICD10 code
K00.5
ICD11 code
LA30.6

No additional description.

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